Annual Report on the Regulatory Flexibility Act, Fiscal Year 2000 20 Years of the Regulatory Flexibility Act Rulemaking in a Dynamic Economy Office of Advocacy U.S. Small Business Administration Washington, D.C.: 2000 ISSN 1047-5168 The full text of this report is available on the Office of Advocacy's Internet site at http://www.sba.gov/advo/. Reprints in paper or microfiche are available for purchase from the National Technical Information Service, 5285 Port Royal Road, Springfield, VA 22161. To the President and Congress of the United States: Twenty years ago, on September 19, 1980, Congress enacted the Regulatory Flexibility Act (RFA) mandating that agencies consider the impacts of regulatory proposals on small entities and determine in good faith whether there were equally effective alternatives that would make the regulatory burden on small business more equitable. In 1996, Congress enacted the Small Business Regulatory Enforcement Fairness Act (SBREFA), amending the RFA in three significant ways. First, courts were given authority to review agency compliance with the RFA in appeals from agency final actions. Second, the Environmental Protection Agency (EPA) and the Occupational Safety and Health Administration (OSHA) were required to convene small business advocacy review panels to consult with small entities when the agency believed it would have to prepare an initial regulatory flexibility analysis of the small entity impacts. Finally, the Chief Counsel for Advocacy's authority to file amicus curiae ("friend of the Court") briefs, authority first granted by the RFA in 1980, was reaffirmed and broadened. This is the seventh report I have submitted since being nominated by the President and confirmed by the Senate in May 1994 as Chief Counsel for Advocacy. I am pleased to report that, although compliance with the RFA still remains somewhat uneven, improved agency compliance is very clearly under way. The Act has become measurably and significantly effective in achieving the law's objective, namely, more equitable regulations. Agencies are learning to do more in-depth and quality regulatory impact analyses and seeking more guidance on how to comply with the RFA. The Office of Advocacy is also now able to estimate the compliance costs that small businesses will not have to incur as the result of regulatory changes made in response to Advocacy's recommendations and those of small business. These regulatory savings amounted to $20.6 billion for the three-year period 1998, 1999, and 2000 and resulted from markedly improved analyses of economic and scientific data urged upon the agencies by Advocacy and others. Agencies should be applauded for their willingness to change regulatory proposals after analyzing both burdensome impacts and alternatives that are equally effective in accomplishing public policy objectives. This, after all, was the result Congress intended when it enacted the RFA. Since enactment of SBREFA, small entities have sought judicial review of agency compliance with the RFA. Not surprisingly, this development has been accompanied by increased agency interest in avoiding challenges to regulations. Last year we reported a noticeable increase in agency requests for Advocacy's guidance on RFA compliance prior to publication of proposals for public comment. This phenomenon was not fleeting. Pre-proposal consultation with the Office of Advocacy has continued and expanded this year. We devoted about 4,300 professional hours this past year to pre-proposal work in addition to the estimated 4,900 hours spent on EPA and OSHA SBREFA panels. These hours also include consultations with the Office of Information and Regulatory Affairs (OIRA) of the Office of Management and Budget pursuant to an "Exchange of Letters" agreed to in January 1995. These consultations have become institutionalized in the close working relationship that has developed from our joint work on SBREFA small business advocacy review panels at EPA and OSHA. On an informal basis, the Office of Advocacy has facilitated meetings for small businesspeople with congressional staff and with executive branch officials, convening ad hoc issue-specific meetings to discuss small business issues. Out of these meetings has emerged the realization that these discussions can lead to smarter regulations and directly benefit the work of regulatory agencies. However, the success of such meetings is directly influenced by the extent to which agency officials are willing to listen. Not all agencies, however, are seeking consultations with the Office of Advocacy or small businesspeople prior to publishing or finalizing proposals, even though some level of outreach to the small business community is required by the RFA. Advocacy has had to critique agency impact analyses and RFA compliance deficiencies, including noncompliance with the Administrative Procedure Act (APA) and the Small Business Act. These criticisms are discussed in Appendix B to this report. espite this uneven performance, significant improvement is under way. As we approach a new Administration and a new Congress, I hope that the progress discussed in this report, marking the 20th anniversary of the RFA, establishes a baseline against which to measure future agency efforts to comply with the law and Advocacy's successes in reducing inequitable regulatory burdens on small business. I will be happy to answer any questions. Just contact me at 202/205-6533. Jere W. Glover Chief Counsel for Advocacy January 2001 Contents Abbreviations Preface Overview: A Brief History of the RFA RFA Compliance Now: How SBREFA Has Changed the Dynamics of Regulatory Development The Future: Unresolved Issues on Which Reasonable People May Differ Conclusion Appendix A: The Regulatory Flexibility Act, as Amended Appendix B: Fiscal Year 2000 Report on Agencies' Compliance with the Regulatory Flexibility Act Appendix C: Regulatory Cost Savings for Fiscal Year 2000 Appendix D: The Regulatory Flexibility Act: Changing the Culture of Federal Agencies Appendix E: Regulatory Comments Filed by the Office of Advocacy during Fiscal Year 2000 Appendix F: Federal Court Decisions Published Since SBREFA Amended the RFA Appendix G: Congressional Testimony Presented by the Chief Counsel for Advocacy during Fiscal Year 2000 Abbreviations ACE-Net Access to Capital Electronic Network AMS Agricultural Marketing Service APA Administrative Procedure Act APHIS Animal and Plant Health Inspection Service ATBCB Architectural and Transportation Barriers Compliance Board ATF Bureau of Alcohol, Tobacco and Firearms BHC bank holding company BLM Bureau of Land Management BPA blanket purchase agreement C.F.R. Code of Federal Regulations CFSAN Center for Food Safety and Applied Nutrition CMRA commercial mail receiving agencies DME durable medical equipment DMERC durable medical equipment regional carrier DOC U.S. Department of Commerce DOD U.S. Department of Defense DOI U.S. Department of the Interior DOJ U.S. Department of Justice DOL U.S. Department of Labor DOT U.S. Department of Transportation EA economic area EO executive order EPA Environmental Protection Agency ERISA Employee Retirement, Income, and Security Act FAA Federal Aviation Administration FAR Federal Acquisition Regulation FCC Federal Communications Commission FDA Food and Drug Administration FDIC Federal Deposit Insurance Corporation FHC financial holding company FHWA Federal Highway Administration FMC Fishery Management Council FMCSA Federal Motor Carrier Safety Administration FNS Food and Nutrition Service FPI Federal Prison Industries FRA Federal Railroad Administration FRFA final regulatory flexibility analysis FRS Federal Reserve System FS Forest Service FSIS Food Safety and Inspection Service FSS Federal Supply Schedules FTC Federal Trade Commission FWS Fish and Wildlife Service GAO General Accounting Office SA General Services Administration GWAC government-wide agency contract HAP hazardous air pollutants HCFA Health Care Financing Administration HHA home health agencies HHS U.S. Department of Health and Human Services HUD U.S. Department of Housing and Urban Development ICANN Internet Corporation for Assigned Names and Numbers IPS interim payment system IRFA initial regulatory flexibility analysis IRS Internal Revenue Service MACT maximum achievable control technology MMS Minerals Management Service MSHA Mine Safety and Health Administration NARA National Archives and Records Administration NASA National Aeronautics and Space Administration NHTSA National Highway Traffic Safety Administration NIST National Institute of Standards and Technology NMFS National Marine Fisheries Service NOAA National Oceanic and Atmospheric Administration NPRM notice of proposed rulemaking NPS National Park Service OASIS outcome and assessment information set OCC Office of the Comptroller of the Currency OFPP Office of Federal Procurement Policy OIRA Office of Information and Regulatory Affairs OMB Office of Management and Budget OSHA Occupational Safety and Health Administration OTS Office of Thrift Supervision P.L. Public Law PCS personal communications services PMB private mail box PPS prospective payment system PRA Paperwork Reduction Act PRO-Net Procurement Marketing and Access Network PWBA Pension and Welfare Benefits Administration RFA Regulatory Flexibility Act RHC rural health clinic RSPA Research and Special Programs Administration SBA Small Business Administration SBREFA Small Business Regulatory Enforcement Fairness Act SBIC small business investment company SEC Securities and Exchange Commission STAWRS state tax and wage reporting system TLD top level domain USDA U.S. Department of Agriculture U.S.C. United States Code USPS United States Postal Service VA U.S. Department of Veterans Affairs WHCSB White House Conference on Small Business WIPO World Intellectual Property Organization Preface On September 19, 1980, the U.S. Congress enacted the Regulatory Flexibility Act (RFA) to ensure that agencies considered the impact of their regulatory proposals on small business.(1) Congress made several findings that frame the overall policy objectives of the law. The most definitive are: "..the failure [by agencies] to recognize differences in the scale and resources of regulated entities has in numerous instances adversely affected competition in the marketplace, discouraged innovation and restricted improvements in productivity; .unnecessary regulations create entry barriers in many industries and discourage potential entrepreneurs from introducing beneficial products and services.."(2) Stated simply, Congress did not want public policy to erect unnecessary barriers to competition; therefore, regulations should not have unintended anti-competitive consequences. Adverse consequences could be avoided if agencies considered the impact of regulations on small business and modified proposals to make them more equitable. It was Congress' intent that this be accomplished without compromising public policy objectives. Over the last past 20 years, there has been significant turnover in policy decision-makers within the Congress, the White House and regulatory agencies. New statutory mandates have been enacted to address societal problems, many of which are complex and identified-as well as solved-by new technology and scientific knowledge. These changes complicate the task of ensuring that there is a consistent approach to complying with the RFA throughout the federal government, while at the same time giving deference to each regulatory agency's expert judgment in crafting regulations that fulfill its public policy mission. Has progress been made? Yes and no. Is the RFA accomplishing its objective? Yes and no. Is the RFA still needed? Definitively, yes. Advocacy is of the view that the RFA is still significantly viable and may always be needed. In an economy that is churning and ever changing, in which new industries emerge or change and in which small business plays such a pivotal role in generating competition, the challenge to avoid unintended consequences from potentially burdensome regulations remains the same as it was in 1980. The reasons the challenge remains the same are several. The government is called upon to address new problems. At the same time, government agencies face an ongoing challenge to craft wise solutions based on sound economic and scientific data, which, in many instances, may not be readily available without additional research. Developing creative solutions to regulatory problems requires appropriate training and resources. Finally, agencies charged by Congress to administer specific laws do not readily see or accept their statutory obligation under the RFA to do no harm to competition by their actions. As a consequence, they do not aggressively pursue analyses of less burdensome alternatives that may be equally effective in fulfilling their public responsibilities. Are changes needed to the RFA? That remains for the readers of this report to answer. This report is intended to present a picture of what exists today that reflects the activities of the Office of Advocacy over the last 20 years. Overview A Brief History of the RFA This report marks the 20th anniversary of the enactment of the RFA-an important milestone. To put the report's contents in perspective, a brief review of some legislative and related history is presented below (see "Important Dates," page 12). Creation of the Office of Advocacy In June 1976, Congress created the Office of Advocacy to be headed by a Chief Counsel, appointed by the President from the private sector and confirmed by the Senate. Congress concluded that small businesses needed a voice in the councils of government -a voice that was both independent and credible-to ensure that big business' influence and well-funded lobbyists did not unduly influence public policy. The Chief Counsel's mandate, therefore, is to be an independent voice for small business in policy deliberations, a unique mission in the federal government, unlike any other. The law specifically required the Office of Advocacy to measure the costs and impacts of regulation on small business. On the regulations, I cannot say enough.somebody has to give us some zip to let it really rip." -James D. McKevitt, National Federation of Independent Business, 1976 Enactment of the Regulatory Flexibility Act (RFA) Studies on the costs and impacts of regulations did not, however, do enough to influence regulatory decisions. Consequently, in September 1980, Congress enacted the Regulatory Flexibility Act (RFA) which mandated that agencies consider the impact of their regulatory proposals on small entities, analyze equally effective alternatives and make their analyses available for public comment. The law was not intended to create special treatment for small business. Congress intended that agencies consider impacts on small business to ensure that, in their efforts to fulfill their public responsibilities, their proposals did not have unintended anti-competitive impacts and that agencies explored less burdensome alternatives that were equally, or more, effective in resolving agency objectives. "Total cost to the U.S. economy of Federal government paperwork requirements is estimated to be $100 billion per year. Private industry cost is $25 to $32 billion per year and it is estimated that 5 million small businesses pay $15 to $20 billion of the $100 billion total. Because of limited resources, small business is woefully ill-equipped to deal with rigid regulatory and paperwork requirements."-Briefing book for the 1980 White House Conference on Small Business The Office of Advocacy was given the responsibility for reporting annually to Congress and the President on agency compliance with this law.(3) The RFA also authorized the Chief Counsel to appear as amicus curiae (i.e. "friend of the court") in actions brought to review a rule.(4) These new responsibilities expanded the role of the Chief Counsel and the office to represent small business in the development of public policy. It was implicitly understood that the effectiveness of these responsibilities was contingent on how well the Chief Counsel asserted the independence that Congress bestowed on the office. Important Dates in the Evolution of the RFA This is a brief chronology of congressional and other actions that have structured or influenced the legal framework within which agencies function to comply with the RFA while fulfilling their statutory mandates. Some of the dates have been highlighted because of their importance. June 1976 Congress enacts Public Law 94-305, creating an Office of Advocacy within the U.S. Small Business Administration charged, among other things, to "measure the direct costs and other effects of federal regulation on small businesses and make legislative and non- legislative pro- posals for eliminating excessive or unnecessary regulation of small businesses." April 1980 The first White House Conference on Small Business calls for "sunset review" and economic impact analysis of regulations, and a regulatory review board including small firm representation. Sept. 1980 Congress passes the Regulatory Flexibility Act (RFA), requiring agencies to analyze the impact of proposed rules on small business, consider and analyze meaningful alternatives, and publish their analyses for public comment. Oct. 1981 The Office of Advocacy reports on the first year of Regulatory Flexibility Act experience intestimony before the Subcommittee on Export Opportunities and Special Small Business Problems of the U.S. House Committee on Small Business. Feb. 1983 Advocacy publishes first in the series of written annual reports on agency RFA implementa- tion. Report shows spotty agency compliance. Nov. 1986 Delegates to the second White House Conference on Small Business recommend strengthening RFA enforcement by, among other things, subjecting agency compliance to judicial review. Sept. 1993 President Clinton issues Executive Order 12866, "Regulatory Planning and Review," requir- ing each federal agency to "tailor its regulations to impose the least burden on society, including businesses of different sizes." Apr. 1994 The General Accounting Office (GAO) issues a report on agencies' compliance with the RFA that concludes: "The SBA annual reports indicated agencies' compliance with the RFA has varied widely.Some agencies.were repeatedly characterized as satisfying the RFA's requirements, while other agencies.were viewed by SBA as recalcitrant.Still other agen- cies' RFA compliance reportedly varied over time.or varied by subagency." June 1995 The third White House Conference on Small Business asks for specific provisions to strength- en the RFA by subjecting additional agencies, including the IRS, to the law; granting judicial review of agency compliance; and including small businesses in the rulemaking process. Oct. 1995 Advocacy submits its report to Congress, The Changing Burden of Regulation, Paperwork and Tax Compliance on Small Business. Data in the report show that small firms with fewer than 20 employees pay 40 percent more in compliance costs than large businesses per dollar of sales; or, measured differently, 33 percent more than large businesses per employee. March 1996 The Small Business Regulatory Enforcement Fairness Act (SBREFA), is signed into law, giving courts jurisdiction to review agency compliance with the RFA, requiring the Environmental Protection Agency and the Occupational Safety and Health Administration to convene small business advocacy review panels, and affirming and expanding the Chief Counsel for Advocacy's authority to file amicus curiae briefs in appeals brought by small entities from final agency actions. 1996-Present Advocacy conducts training sessions for more than 2,000 trade association executives and federal officials. Jan. 7, 1998 Advocacy files its first amicus curiae brief and the court remands the challenged rule to the agency on March 13, 1998. For 15 years, the Chief Counsel reported rather graphically that compliance with the RFA was uneven throughout the government. This was confirmed by the General Accounting Office's (GAO) study in April 1994, cited in the chronology. Recognition was growing that some "teeth" needed to be added to the RFA. This would provide more incentive for agencies to comply with Advocacy's congressional mandate deemed so important to the national economy. Enactment of the Small Business Regulatory Enforcement Fairness Act (SBREFA) In March 1996, the Small Business Regulatory Enforcement Fairness Act (SBREFA) became law. SBREFA raised the stakes for regulatory agencies. Congress had finally been persuaded by 15 years of uneven compliance with the law, and by the repeated urging of the small business community, to authorize the courts to review agency compliance with the RFA. "Judicial review" was thought to be the incentive that was lacking in the original statute. SBREFA also reinforced the RFA requirement that agencies reach out to small entities in the development of regulatory proposals, subjecting this outreach to judicial review as well. "Clearly, SBREFA provided much needed `teeth' to the RFA by.allowing for judicial review of selected portions of the RFA. This is a powerful tool for the small business community and has empowered small business.to fight oppressive regulations effectively."-Laura Skaer, Northwest Mining Association Very explicit outreach responsibilities were imposed on the Environmental Protection Agency (EPA) and the Occupational Safety and Health Administration (OSHA). These two agencies are required to convene small business advocacy review panels that consult with small entities on the overall effectiveness and impacts of specific proposals.(5) This precedent-setting provision of the law institutionalizes outreach to small entities and ensures that these two agencies identify and consider effective alternatives that accomplish their public policy objectives. The Chief Counsel for Advocacy and the Office of Information and Regulatory Affairs (OIRA) of the Office of Management and Budget (OMB) are statutory members of the panels and are mandated to partner with these agencies to consult with small entities on regulatory proposals. They report their findings, jointly with agency staff, to the head of the agency. Advocacy and OIRA have access-by act of Congress-to an agency's earliest deliberations that identify a problem, document the scope of the problem, analyze its various causes, and evaluate how best to address the problem without unnecessary harm to small business or the economy. From a statutory perspective this overview brings us to today- four years after the passage of SBREFA and 20 years after enactment of the Regulatory Flexibility Act. The balance of this report reviews: RFA Compliance Now The value of outreach to small business-RFA mandates The role of economic and scientific data Amicus curiae authority The significant economic impact of RFA, as amended by SBREFA RFA Winners, Honorable Mentions and Agencies in Need of Improvement The Future-What Lies Ahead Conclusion RFA Compliance Now How SBREFA Has Changed the Dynamics of Regulatory Development The RFA has meant different things to different agencies. Some have viewed it as merely a procedural law-a checklist or a legal hoop to jump through-compliance with which could easily be achieved if agencies just crossed the t's and dotted the i's. Some agencies did not view it as having mandated an analytical process to be customized to an agency's mission. Some failed to understand that RFA's mandates did not lend themselves to a "cookie cutter" approach, or that the RFA specifically was designed to eliminate a "one-size-fits-all" approach to regulation. Some chose to ignore the law's mandates altogether, at least initially. Most agencies found compliance with the RFA to be a difficult and useless exercise, in part because they were at the bottom of the learning curve on how to do the kind of impact analyses required by the RFA. They also resisted appropriate analyses because they believed the law gave special treatment and an unfair advantage to small business. Other agencies have taken substantial steps to comply with both the letter and spirit of the RFA.(6) Judicial Review SBREFA, which has been in effect for four years, has started to change these dynamics. Advocacy is convinced that the impetus for the change comes from the amendment that allows the courts to review agency compliance with the RFA. This, in combination with the Chief Counsel's authority to file as amicus curiae in regulatory appeals, provides a powerful incentive for agencies to reduce the risk of having their rules judicially challenged in court and remanded for failure to comply with the RFA. "One could say this litigation under the RFA has been a "learning experience" for the agency. Our efforts to comply with the Regulatory Flexibility Act, though well intentioned, have not always met with judicial favor. We recognize that there is room for improvement in our economic analyses, and I would like to describe the steps we are taking to make them better."-Testimony of Penelope Dalton, Assistant Administrator for Fisheries, National Marine Fisheries Service, before a subcommittee of the U.S. House of Representatives; April 29, 1999 It appears that the threat of judicial review is making agencies acutely aware of the need to perform regulatory impact analyses. By performing regulatory analyses, even with incomplete data, some agencies have begun to recognize that early review of rules for potential small business impacts results in more informed decision-making. More agencies are beginning to provide more factual information, as required by the RFA, to justify their certifications that rules will not have a significant economic impact on a substantial number of small entities. Regulatory flexibility analyses, and the economic data that supports them, are also showing real improvement. At the same time, the OSHA and EPA small business advocacy review panels are clearly demonstrating the value of early consultation with small entities. Rules have been modified and compliance costs reduced. The panels are providing concrete evidence that rulemaking that analyzes small entity impacts does not compromise public policy and results in more workable and reasonable rules. These changes are the result of: small businesses challenging rules and requesting judicial review of agency compliance with the RFA; and Advocacy's first amicus curiae brief filed in a case that resulted in the remand of a rule to the regulatory agency. "The concerns of the small business community are important to the CPSC. The Commission has made significant efforts to reach out to small businesses and consider the impact of our activities on them."-Thomas W. Murr, Jr., Deputy Executive Director, U.S. Consumer Product Safety Commission (CPSC). It is safe to say that federal agencies today are finally beginning to do what they should have been doing since the RFA first became law in 1980: considering small business concerns as rules are being developed-not as an afterthought. Pre-Proposal Consultation-The Major Change One of the more significant changes that emerged just in the past year is the amount of consultation agencies have sought with Advocacy prior to publication of a rule for public comment. In FY 2000, the amount of pre-proposal activity in which Advocacy has participated has dramatically increased. Advocacy estimates that approximately 18 percent of the regulatory staff's time has been spent on pre-proposal work (an estimated 4,300 hours), exclusive of the staff time spent on SBREFA EPA and OSHA panels.(7) "...[D]uring a recent DOT.....rulemaking, the Office of Advocacy played the leading role in persuading the agency to reverse their negative small business effect certification. By this action the entire nature of the rulemaking was changed to the benefit of small coach operators."-Norm Littler, United Motorcoach Association An ever-increasing number of agencies are contacting Advocacy with questions about potential RFA problems and small business economic impact analyses.(9) This type of early consultation has led to the development of better rules, namely, rules that accomplish the agencies' public policy goals while avoiding undue burdens on small entities. When Advocacy has been successful in altering a proposal prior to publication, the need to submit comments for the public record has been eliminated. This shift to pre-proposal work is productive for agencies, for Advocacy, and most important, for small business. Time and again Advocacy has successfully identified weaknesses in agency analyses before publication. It has also demonstrated how to provide information that would be the most useful to the public in order to elicit informed submissions from the public during the comment period. This early attention to RFA compliance issues helps reduce the overall cost of regulatory development and the risk that a rule will be judicially challenged. There is no question that a rule that goes through this process results in more informed public policy. To illustrate: Advocacy worked with an agency in the Department of Transportation (DOT) on a rule affecting small business. This partnership resulted in the agency altering its conclusion that the rule would not significantly affect small entities. Instead, DOT made a commitment to analyze the possible economic impacts further. The Forest Service agreed to perform an initial regulatory flexibility analysis (IRFA), as required by the RFA, after Advocacy reviewed its draft proposal during early consultation and persuaded the agency that the rule would in fact have an impact on small commercial operations as well as on small communities. The Minerals Management Service dramatically improved the justification for its RFA certification so that the public was able to provide useful comments on the accuracy of the agency's determination. These are just a few of the many ways in which Advocacy's work on agency compliance with the RFA is extremely beneficial-and cost effective-when done at the pre-proposal stage of regulatory development. The Value of Outreach to Small Entities-RFA Mandates When the RFA was enacted in 1980, Congress established procedures for agencies to follow to ensure that small entities would have the opportunity to participate in the rulemaking process.(9) These procedures included direct notification to affected entities and measures to reduce the cost or complexity of participation. Congress' clear intent was that small entities should be at the regulatory table and that the process should be made easy for them. This mandate was also in response to the reality that large business has well-financed lobbyists with fine-tuned government networks through which they can work very effectively to influence public policy, sometimes to the detriment of other sectors in the economy. Special interests also have ready access to other vehicles through which to make their voices heard, such as government advisory committees, negotiated rulemaking, subsidized industry conferences, etc. Given this reality, complaints that suggested outreach to small business gave it an unfair advantage are unfounded. The mandates merely balance the scales. With the SBREFA amendments Congress took the mandated outreach process one step further. Small Business Advocacy Review Panels- The Outreach Process Mandated for EPA and OSHA In 1996, SBREFA mandated that whenever EPA or OSHA finds that a regulatory proposal may have a significant economic impact on a substantial number of small entities, the agency is required to convene a panel and prepare a regulatory flexibility analysis. The review panel consists of representatives from the rulemaking agency, Advocacy, and the Office of Information and Regulatory Affairs within the Office of Management and Budget. The panel conducts its own outreach to small entities likely to be affected by the proposal, seeks their input on the proposed regulation, and prepares a report to either the EPA or OSHA with recommendations for reducing the potential impact of the rule on small businesses. The panel has 60 days in which to submit a report on its findings, which becomes part of the public rulemaking record. After the report is received, the agency may reconsider its proposal or modify it in response to the information received. To date, work has been completed on 24 small business advocacy review panels-21 EPA panels and 3 OSHA panels (Table 1). Table 1. SBREFA Panels through Fiscal Year 2000 Rule Subject Date Report NPRM Convene Completed d Environmental Protection Agency Panels Non-Road Diesel Engines 03/25/9 05/23/97 09/2 7 4/97 Industrial Laundries Effluent 06/06/9 08/08/97 12/1 Guideline 7 2/97 Stormwater Phase 2 06/19/9 08/07/97 01/0 7 9/98 Transport Equipment Cleaning 07/16/9 09/23/97 06/2 Effluent Guideline 7 5/98 Centralized Waste Treatment 11/06/9 01/23/98 01/1 Effluent Guideline 7 3/99 Underground Injection Control 02/17/9 04/17/98 07/2 Class V Wells 8 9/98 Ground Water 04/10/9 06/09/98 05/1 8 0/00 Federal Implementation Plan for 06/23/9 08/21/98 09/3 Regional Nitrogen Oxides 8 0/98 Reductions Section 126 Petitions 06/23/9 08/21/98 09/3 8 0/98 Radon in Drinking Water 07/09/9 09/18/98 11/0 8 2/99 Long Term 1 Enhanced Surface 08/21/9 10/19/98 04/1 Water Treatment 8 0/00 Filter Backwash Recycling 08/21/9 10/19/98 04/1 8 0/00 Light Duty Vehicles/Light Duty 08/27/9 10/26/98 05/1 TrucksEmissions and Sulfur in 9 3/99 Gas Arsenic in Drinking Water 03/30/9 06/04/99 06/2 9 2/00 Recreational Marine Engines 06/07/9 08/27/99 In 9 proc ess LDV/LDT Emissions and Sulfur In 08/27/9 10/26/98 05/1 Gas 8 3/99 Diesel Fuel Sulfur Control 11/12/9 03/24/00 06/0 Requirements 9 2/00 Lead Renovation and Remodeling 11/23/9 03/03/00 In Rule 9 proc ess Metals Products and Machinery 12/09/9 03/03/00 In 9 proc ess Concentrated Animal Feedlots 12/16/9 04/07/00 In 9 proc ess Reinforced Plastics Composites 04/06/0 06/02/00 In 0 proc ess Stage 2 Disinfectant Byproducts 04/25/0 06/23/00 In 0 proc ess Occupational Safety and Health Administration Panels Tuberculosis 09/10/9 11/12/96 10/1 6 7/97 Safety and Health Program Rule 10/20/9 12/19/98 In 8 proc ess Ergonomics Program Standard 03/02/9 04/30/99 11/2 9 3/99 Note: NPRM = Notice of Proposed Rulemaking Because EPA has worked on more panels, it has been able to fine- tune the process to ensure that the right kinds of information and analyses are made available to the small entities to be consulted by its panels. EPA's performance has not always been consistent across the board, but on the whole its record surpasses other affected federal agencies. "Each of the 15 complete SBREFA panels has resulted in positive outcomes for the Agency and small businesses. In each case the Panel's report has included concrete recommendations to the Administrator for her to consider in the development of the subject rule."-Thomas E. Kelly, U.S. Environmental Protection Agency. To date, approximately 400 small entities have been consulted on a very diverse array of rules. The additional input from small entity representatives has spotlighted real-life consequences of proposals under consideration. In nearly every instance to date, information provided by small entities, in combination with other data, has proven invaluable in establishing a reality check for these agencies, namely, what the real impact of the regulation is likely to be and the actual compliance costs small entities will have to bear. Regulations that have emerged from the panel process have been changed in response to the concerns of small business and are less burdensome than the regulations initially considered by the agency. In one instance, a regulation was withdrawn entirely because the data clearly demonstrated that there was no need for national regulation, saving small businesses approximately $103 million annually.(10) All of these significant changes have resulted in rules that are less burdensome on small entities without compromising the public policy objectives of the agencies. "I was a small entity representative for industry in the SBREFA processes and worked closely with [Advocacy]...to reduce the impact of [EPA] regulations. Together we have established precedent-setting regulations and procedures that will likely save the regulated community several hundred million dollars annually."-Jack Waggener, URS Corporation. Although work on the panels has been productive, it has also been labor-intensive. For the seven panels completed in FY 2000, Advocacy alone spent an average of 700 hours per panel-for a total of 4,900 hours.(11) While time-consuming for Advocacy (and OIRA), once the analytical process becomes part of the agency's regulatory culture, agencies subject to the SBREFA panel process should not experience any additional burden over and above what they are already required to do under the Administrative Procedure Act (APA). Advocacy has consistently maintained that the analysis required by the RFA in preparation for a SBREFA panel is not an additional burden. Rather, it is exactly the kind of analysis an agency is already mandated to do by the APA. What the RFA added to the process was a congressional mandate to consider explicitly the impacts on small business, which agencies should have been doing all along, in order to avoid harming competition unnecessarily. "[F]ollowing the small business panel session on ergonomics, the Office of Advocacy brought to light some major deficiencies with OSHA's draft ergonomics proposal and the difficulty industry will have to comply with the rule." -Don E. Gaertner, American Foundry Society. Any additional work that may be needed to complete the 60-day panel process is offset by time saved at the other end of the regulatory process. When problems are resolved prior to publication, objections from the public are reduced and less time must be spent crafting responses. All of the rules reviewed by EPA and OSHA SBREFA panels that have now been finalized were modified significantly to mitigate unnecessary and unproductive burdens on small business and to eliminate unworkable provisions. Even OSHA's controversial ergonomics final rule, though much criticized by small business, was changed dramatically as a result of the input from small business during the SBREFA panel process. Without that crucial step in the rule's development, the pre-panel draft of the rule would most likely have become the proposed rule, costing small businesses even more in compliance costs. SBREFA panels continue to be an important mandate of the RFA that ensures small business a formal seat at the regulatory table, where their input can and does make a real difference. Advocacy's Outreach to Small Entities In addition to its work on panels, Advocacy hosts roundtable discussions to gather information on current trends and regulatory impacts from small businesses themselves. When monitoring agency compliance with the RFA, it is useful for Advocacy to understand the impact of proposed regulations on specific industries. Frequently, the necessary historical data on those industries does not exist. In order to develop some knowledge about current industry structure, etc., these industry- specific roundtable meetings have been convened by Advocacy to discuss pending issues on an ad hoc basis with small business representatives. Representatives from relevant regulatory agencies and congressional committee staff have also been invited to participate. The meetings have uniformly been viewed as helpful in identifying and raising awareness of small business issues. "Through the Small Business Regulatory Enforcement Fairness Act (SBREFA) of 1996, your office has provided small business a stronger voice in the federal regulatory process."-Don E. Gaertner, American Foundry Society The Role of Economic and Scientific Data Not all policymakers understand or accept the important role played by small business in maintaining competition. Too often they are familiar only with the literature produced by business schools and research addressing big business issues. The adverse long-term impacts of industrial concentration on price, innovation, and choice are not readily understood. This lack of understanding complicates the task of persuading agencies-often focused on other important but more narrow policy missions-that they are also responsible for the larger national policy objective of preserving competition. More specifically, this means "do no undue harm to small business." It is a well-established economic axiom that "information rationalizes markets." Information also rationalizes public policy. This is one of the underlying reasons that Congress mandated that agencies reach out to small businesses and involve them in the process. As noted earlier, small business input on SBREFA panels has been a major influencing factor in fashioning more workable regulations. The information obtained from these small businesses themselves, though vital, is generally anecdotal. The challenge before agencies and the Office of Advocacy is to develop statistically sound data (both economic and scientific) that document the existence, scope and causes of a problem. Additional important information assesses who the responsible parties are and the extent of their contribution to a problem. This analysis leads to an intelligent determination of how the causes can be remedied by regulation. Much of Advocacy's time in connection with SBREFA panels is spent reviewing agency data and having it validated or challenged by independently obtained data. The importance of data to the regulatory process and rational decision-making cannot be overemphasized. It was data that persuaded EPA to drop an industrial laundries water pollution regulation that saved small businesses approximately $103 million annually. The data showed there was no need for a national rule. It was data that convinced OSHA that its compliance cost estimates were too low for its ergonomics rule.(12) Advocacy anticipates that one of the benefits that will emerge from early consultation with agencies on RFA issues will be increased awareness of what agencies do not know-but should know-about the industries they are trying to regulate. This will help agencies understand how the regulatory process aids in eliciting relevant information from the public. Further, agencies unwittingly fail to use, or chose to ignore, readily available in- house information (e.g., company data submitted to obtain licenses, etc.). For now, Advocacy issues task order contracts to researchers who are hired on a task-by-task basis to analyze data in connection with specific rules. This increases Advocacy's flexibility. It avoids the need to hire full-time staff with narrow specialties to perform tasks that can be more readily obtained at less cost to the taxpayer through a contractor for the short period of time needed to analyze a rule.(13) Partnership with the Office of Information and Regulatory Affairs (OIRA) On January 11, 1995, the Office of Information and Regulatory Affairs (OIRA) of the Office of Management and Budget (OMB) and Advocacy signed an "Exchange of Letters" outlining how both agencies would work together on regulatory issues. In those letters Advocacy agreed to contact OIRA whenever it had concerns about an agency's compliance with the RFA. OIRA in turn agreed that it would consult with Advocacy when it was not able to resolve RFA issues with an agency. The SBREFA panel process brought Advocacy and OIRA even closer together, and from this relationship a mutual respect has developed. OIRA is also responsible for ensuring agency compliance with Executive Order 12866 and the Paperwork Reduction Act, both of which concern Advocacy from a small business perspective.(14) Increasingly, OIRA is sharing agency rulemaking drafts with Advocacy in order to obtain initial comments on an agency's RFA compliance as part of the EO review. This early access to important agency information enables Advocacy to comment at a vital stage of the rule's development and have an impact on its final design. Prior to promulgation of a final rule, Advocacy often participates in meetings and discussions with both OIRA and the relevant regulatory agency, in order to advocate for crucial RFA- mandated changes on behalf of small business. This important working relationship with OMB at all stages of a rule's development has assisted the Office of Advocacy in monitoring agency compliance with the RFA more closely. This new and improved working relationship has been mutually beneficial. Amicus Curiae Authority Section 612 of the RFA vests in the Chief Counsel for Advocacy the authority to appear as amicus curiae (i.e., "friend of the court") in any court action to review a rule. Specifically, the Chief Counsel is authorized to present views with respect to compliance with the RFA, the adequacy of a rulemaking record pertaining to small entities, and the effect of rules on small entities. Under this section of the RFA, courts are bound to grant the amicus curiae application of the Chief Counsel. This section of the RFA existed prior to SBREFA, albeit in a slightly different form. Prior to the 1996 SBREFA amendments, some argued that the section limited the Chief Counsel's authority only to reviewing the effects of a rule on small entities. In this context, the courts were bound to grant the amicus curiae application of the Chief Counsel. However, this very general authority did not explicitly allow the Chief Counsel to raise RFA issues because there was no judicial review of RFA actions prior to SBREFA. Consequently, the Chief Counsel had to use creative means to enter his appearance in court actions if he wanted to challenge a regulation based on an agency's failure to comply with the RFA. For instance, in 1994, the Office of Advocacy prepared an amicus curiae brief in the case of Time Warner Entertainment Company v. FCC, 56 F.3d 151 (D.C. Cir. 1995), cert. denied, 516 US 112 (1996). The Chief Counsel argued, among other things, that noncompliance with the RFA was arbitrary and capricious under the Administrative Procedure Act. After last- minute negotiations, the FCC agreed to alter its policy and Advocacy withdrew its notice of intent to file. "It is our opinion that the Office of Advocacy's interventions into our case and the subsequently filed amicus brief in support of our position challenging the regulations clarified the issues for resolution by the court. The Office of Advocacy's brief was very persuasive to the court's favorable interpretation of the RFA and SBREFA in accordance with congressional intent."-Laura Skaer, Northwest Mining Association. As the Time Warner case demonstrates, the threat of filing a brief in court is sometimes sufficient to persuade an agency to change its course. For instance, in the case of Grand Canyon Air Tour Coalition v. FAA, 154 F.3d 455 (D.C. Cir. 1998), Advocacy withdrew its notice of intent to file a brief in exchange for an agreement with the U.S. Department of Transportation (DOT). The agreement required DOT to submit to the court a statement detailing new data regarding the number of aircraft subject to the regulation. Further, DOT was to include in its communication to the court a statement that the agency erroneously certified that the final rule would not have a significant economic impact on a substantial number of small entities. In Southern Offshore Fishing Association v. Daley, 995 F. Supp. 1411 (M.D. Fla. 1998), Advocacy withdrew its notice of intent to file after it was able to obtain an agreement from the Department of Justice (DOJ) that the proper standard of review in RFA cases is the "arbitrary and capricious" standard. This acknowledgment from DOJ was significant-not only because it conceded the use of the appropriate standard, but also because it implicitly accepted Advocacy's authority to file amicus briefs. This was an important concession, as DOJ had always objected to Advocacy's right to file such briefs in the past. Advocacy has filed one amicus curiae brief since passage of SBREFA. Northwest Mining Association v. Babbitt, 5 F. Supp. 2d (D.D.C. 1998), involved a hardrock mining rule with a number of major defects. Advocacy argued that major new costly requirements were being introduced for the first time after a 6-year delay in issuing a final rule, and the agency's analysis was confusing and inadequate. The court chose to focus on the fact that the agency failed to comply with the definition of a small entity as defined in the RFA and the Small Business Act. Primarily because of Advocacy's arguments, the rule was remanded to the agency. Advocacy uses its amicus curiae authority judiciously. Since Advocacy is not a litigation office, the time needed for writing a brief can present a strain on the office's resources. Therefore, in assessing whether to file a brief, Advocacy has established certain criteria. Two of the main criteria are whether the office can make a difference by getting involved and whether small business views will be adequately represented by others. The second criterion is derived from the fact that courts will not generally accept duplicative arguments made by amicus curiae. The Significant Economic Impact of the RFA, as Amended by SBREFA Given the uneven performance by agencies over the last 20 years, legitimate questions may be posed about the RFA. How effective has the RFA been? Has it been a total failure? What measures should be used to gauge the law's effectiveness? These questions need to be answered, if for no other reason than to overcome agency skepticism about the true meaning of the law. For the past three fiscal years Advocacy has measured the difference between the compliance costs of an original regulatory proposal and those associated with the rule that ultimately emerges from the regulatory process. The difference between these costs measures the extent to which regulatory impact analyses (compliance with the RFA) altered the policymakers' views of how best to solve a problem. This measurement is termed "regulatory savings" (Table 2). Table 2. Regulatory Savings (1) (2) (3) One-Time Annual Cumulative Total Fiscal Savings Savings Annual (1) plus Year Total (3) FY 1998 $0 $3.2 $9.6 $9.6 billion billion billion (3 years) FY 1999 $ 3.0 $2.2 $4.4 $7.4 billion billion billion billion (2 years) FY2000 $3.2 $ .4 $.4 $3.6 billion billion billion billion TOTAL $6.2 $5.8 $14.4 $20.6 billion billion billion billion three-year total Notes: See Appendix B for more information about the regulations that generated these savings. Some savings to small businesses are a one-time savings of costs avoided in one year (1). Others are saved by small businesses every year (2). The cumulative annual total in column (3) represents the annual savings times the number of years in which those savings have occurred, up to FY 2000. While the three-year total of $20.6 billion in regulatory savings does not directly deposit any monies into the coffers of small business, the savings do represent monies small business did not have to expend on compliance with regulations. These figures dramatically highlight that compliance with the RFA does have a positive impact and does avoid unnecessary costs for small business. Agencies are to be applauded for adjusting their proposals when sound analyses dictate such an outcome. On the other hand, the figures also demonstrate that agencies need to do more analyses in advance of proposing regulations-which after all is the intent of the RFA. Interestingly, the cumulative three-year total represents a return of between $1144 and $1373 for every dollar spent on Advocacy's total budget for the past three years, assuming that Advocacy's budget (including salaries, expenses and research funds) is between $5 and $6 million per year.(15) The RFA Winners, Honorable Mentions, and Agencies in Need of Improvement In the preface of this report, Advocacy noted that there has been significant turnover in the policy decision-makers within the federal government. In addition, some agencies promulgate more rules than do others; some have a spate of rules in one year, but none in another year. These factors partially explain why compliance with the RFA by agencies and some sub-agencies of major departments has been uneven over the years. Until SBREFA, there was no real incentive to institutionalize the analytical process mandated by the RFA. Despite SBREFA, uneven compliance exists today, although Advocacy perceives some improvements in agency efforts to comply with the law. Some agencies fail consistently to provide factual bases for their certifications that rules will not have a significant impact on a substantial number of small businesses. Others fail miserably in analyzing the impact of rules on small business, or fail to make their analyses transparent, thus frustrating the public's ability to assess the validity of the analyses or to pinpoint flaws in agency reasoning. Still others use boilerplate language either in certifications or in their analyses. Too many agencies still do not consider small business impacts as they are developing rules and address the issue only after the fact. Some agencies are learning the hard way-after court challenges-that there is a better way to develop rules. Some agencies are learning by observation. They watch what happens to other agencies that ignore the RFA. Agencies on the top of the learning curve quickly grasp how proper analyses can help them develop smarter rules. In previous reports, Advocacy has discussed in some detail the contents of communications submitted for the record in various rulemakings. This year, that discussion is contained in Appendix B. The information contained therein provides a comprehensive overview of the diverse agencies and issues with which Advocacy has dealt in the past year. In reviewing this appendix it is important to appreciate that it contains information only on documents that are a matter of public record and does not contain any of the information or work product generated during interagency nonpublic pre-proposal discussions. This year, in light of the RFA's 20th anniversary, Advocacy thought it appropriate to recognize those agencies that have made the most progress (Winners), agencies that have made some progress worth noting (Honorable Mentions) and those agencies whose performance needs significant improvement. The following criteria were used to select agencies for recognition: Anticipating RFA problems and seeking guidance; Good faith outreach to small business; Adequate factual information to substantiate certifications; Well-documented regulatory flexibility analyses; Factual presentation of data on the structure and economics of the industry being regulated; Good-faith efforts to elicit information during the rulemaking process to supplement agency data; Compliance with the Small Business Act's and the RFA's size standards and the process for seeking exceptions; Consideration and evaluation of truly meaningful alternatives-not just alternatives that would never be seriously considered; Meaningful responses to Advocacy's critiques of regulatory proposals. The RFA Winners The Office of Science and Technology-EPA. The Office of Science and Technology is a division within the Environmental Protection Agency. This division has shown exemplary compliance with the objectives of the RFA during FY 2000. Its data and analyses have been extremely comprehensive, thus establishing a high level of credibility in the work of the staff. Its analytical work should serve as a model for the rest of EPA. The Office of Science and Technology has shown the ability to work effectively with the Office of Advocacy and industry during the promulgation of its rules. This relationship was instrumental in assuring significant cost savings on two rules: the metals products and machinery rule (panel completed in March 2000 and rule proposed in December 2000) and the transportation equipment cleaning rule (rule completed in August 2000). As a result of the cost savings generated by the two rules, Advocacy expects annual savings in excess of $100 million. The Center for Food Safety and Applied Nutrition-HHS. The Center for Food Safety and Applied Nutrition (CFSAN), a division within the Department of Health and Human Services, is lauded for its efforts to help small entities. CFSAN has worked with Advocacy by offering briefings on upcoming regulations that will affect small entities before the regulations are even proposed. CFSAN seems to have made an institutional adjustment and a conscious decision to analyze thoroughly the impact of its regulations on small entities, thereby mitigating adverse impacts where possible. This institutional change came about after several harsh comments submitted earlier by Advocacy criticizing CFSAN's analyses and its failure to comply with the RFA. Officials from CFSAN have stated that it is more productive to work with Advocacy in the earliest stages of rule promulgation than against Advocacy after a negative comment has been received. It is Advocacy's hope that CFSAN will maintain these practices when issuing new regulations on dietary supplements-regulations that contained RFA compliance problems in the past. The Employee Benefits Office-Treasury Department. The Employee Benefits Office of the Treasury Department has made a special effort to respond to the small business community. During the last year, Advocacy has worked with the Employee Benefits Office and Treasury in an effort to resolve two major issues: more flexibility for small business 401(k) plans and comparability testing for defined contribution plans and benefits. The office has made an effort over the last five years to work with small business to simplify small business pension plans and increase benefits to reflect real retirement needs. Ultimately the efforts of the Employee Benefits Office have increased pension participation. Securities and Exchange Commission. The Securities and Exchange Commission (SEC) has always maintained a positive relationship with the Office of Advocacy. The two agencies have long worked closely at the pre-proposal stage (and generally) to assure that SEC's policies remain sensitive to small business concerns. The SEC also is diligent in complying with RFA's size standards requirements and arguably has the best record of adhering to the statutory process for obtaining exceptions. In addition, the SEC can be commended for various efforts to reach out and include small businesses in its regulatory processes, including its successful Government Business Forum on Small Business Capital Formation. Information gleaned at this forum has had a direct impact on SEC regulations and policies. The RFA Honorable Mentions Two agencies have made noteworthy progress and deserve recognition for their efforts, even though more needs to be done to make them "winners." Internal Revenue Service. The SBREFA extended the RFA to IRS interpretive rules that impose recordkeeping requirements. IRS has interpreted this provision narrowly and has certified rules that would impose de facto recordkeeping burdens. By the same token, it has on other occasions performed regulatory flexibility analyses when a rule explicitly imposed a recordkeeping burden. Advocacy is of the view that the IRS should be more sensitive to de facto burdens and perform more analyses. The Department of the Treasury and the IRS have made an informal effort to reach out on regulations where it can be ascertained that a high-visibility problem exists for small businesses. In areas involving controversial definitions (such as worker classifications), cash versus accrual accounting, employment reporting, tip reporting, capitalization rules, and other industry-specific problem areas, the IRS has made a significant effort to appreciate small business concerns. The IRS and Treasury have become more amenable to gathering small business input before promulgating regulations. Such an informal effort is an encouraging sign, even if the IRS and Treasury continue to resist following the formal requirements of the RFA and SBREFA (see Appendix B). National Marine Fisheries Service. Although Advocacy recognizes that the National Marine Fisheries Service (NMFS) still has work to do, it would be unfair not to recognize the efforts that NMFS has made to comply with the spirit of the RFA. After the passage of SBREFA, several NMFS regulations were challenged for failure to comply with the requirements of the RFA. In response to the judicial review provisions in SBREFA, NMFS began to work with Advocacy to improve its RFA compliance. By working with Advocacy on matters of concern, NMFS has addressed issues and, in some instances, like the regulations concerning "spotter planes" and the Florida Keys sanctuary, has avoided judicial review or overcome the court challenge Noteworthy is the decision to make institutional changes in the manner in which they approached the RFA. Whereas they initially had standards to determine "significant" and "substantial," those standards were abandoned in an effort to encourage their regulators to perform an economic analysis, as opposed to simply certifying the rule and using the standards to justify the certification. NMFS consulted with Advocacy in developing the guidelines and also published them for public comment. NMFS has distributed the guidelines to all of their offices and is also providing training sessions for their regulators. NMFS should also be lauded for hiring an economist and an attorney specifically to work on RFA issues and to be a point person for their regulators in terms of RFA guidance. In addition, NMFS has made significant attempts to increase their outreach to small entities. In addition to hiring an ombudsman to address small entity concerns, NMFS has made a concerted effort to send representatives to Advocacy roundtables. At the roundtables, NMFS listens to the concerns of the industry, explains the basis for some of its actions, and attempts to clarify misunderstandings. For example, at one roundtable, NMFS learned that some of the regional personnel would not provide fishers with information about quotas if the matter was the subject of litigation. NMFS immediately addressed the problem by instructing the regional staff to provide the information and explaining which types of information can be released when a particular fishery may be the subject of litigation. While the relationship between the industry and NMFS may be somewhat strained, it is hoped that continued open exchange of information and institutional changes will improve that relationship. Agencies in Need of Improvement Some agencies exhibit compliance problems in some or all aspects of the RFA. Advocacy has tried to work with these agencies; has submitted public comments that were very explicit about the agencies' RFA deficiencies; but the agencies still need to apply the requirements of the RFA with greater consistency. Having said this, Advocacy nevertheless wishes to extend an invitation to these agencies to develop a working relationship that will benefit the regulatory process, help small business, and produce smarter regulations. It would be Advocacy's goal to be able to characterize them as "winners" in next year's report. The Federal Communications Commission. The Federal Communications Commission (FCC) is notorious for its poor compliance with the RFA. Although the FCC frequently provides detailed insight into the purposes and rationale underlying a rule, it offers only cursory discussion of a rule's impact on small business. The FCC's regulatory flexibility analyses are invariably cut-and- paste, offer no real insight, and are entirely divorced from the "substantive" portions of the rulemaking. The FCC also violates requirements governing size standards for small businesses established under the Small Business Act. The agency has established a general pattern of changing size standards as it sees fit, often approaching SBA to seek an exception only after it has adopted a new size standard. Advocacy recognizes the limited discretion FCC staff is allowed to exercise within an agency where decisions are made by a collegial body. This does not excuse the commission itself, however, since it has been made well aware of its legal responsibilities under the RFA. Although there have been several training sessions for commission staff, including staff of the commissioners, Advocacy sees little evidence that change is occurring to improve compliance. The Health Care Financing Administration-HHS. The Health Care Financing Administration (HCFA) is a division within the Department of Health and Human Services. Despite HCFA's challenging congressional mandate to implement major Medicare reforms within short statutory deadlines, Advocacy believes that it could do a better job of considering less burdensome regulatory alternatives that still meet statutory requirements and of following administrative procedures that require public notice and comment. Also, many health care providers have expressed great frustration with HCFA and some of the practices of its regional carriers, in particular. It is hoped that HCFA will rid itself of this negative public perception by looking more closely at regulatory alternatives and by forcing its regional carriers to apply HCFA's guidelines with significantly greater consistency. Advocacy has heard many complaints, past and present, regarding the inconsistency with which HCFA's regional carriers apply HCFA's guidance in processing provider claims. Many small businesses have complained that the regional carriers abuse their discretion, delay claims unnecessarily and otherwise process claims in an arbitrary fashion, with differing processing practices across the country. HCFA should make every attempt to reign in abusive and inefficient carriers. In the past, HCFA had developed the practice of publishing rules as direct and interim final rules. This was the case in several major regulations like the ones for surety bonds for home health agencies, the interim payment system for home health agencies, and inherent reasonableness. Doing so allowed the agency to bypass notice and comment procedures required by the Administrative Procedure Act. The agency also requested expedited OMB review of paperwork requirements in a situation Advocacy believed did not warrant such a procedure. In this particular case, Advocacy had already submitted comments criticizing a similar action by the agency in an analogous situation the previous year. In both situations-issuing direct final rules and requesting expedited OMB review-affected entities are precluded from commenting on the potential effects of the rule. Finally, on the issue of alternatives, Advocacy continues to work with the agency to devise less burdensome alternatives in its regulations. For instance, Advocacy continues to urge the agency to provide an analysis and regulatory alternatives for its rule that deals, in part, with the length of time patients can be restrained in a medical facility. A court has also ruled that this analysis is required. HCFA has made progress in its RFA compliance efforts recently, and is beginning to consult Advocacy early on some controversial regulations. The Food and Nutrition Service-USDA. The Food and Nutrition Service (FNS) is a division within the U.S. Department of Agriculture. At least twice in FY 2000, FNS certified that its regulations would not have a significant economic impact on a substantial number of small entities. However, there was no factual basis for the certifications. FNS does not discuss the number of small entities affected by the rule-an RFA requirement for determining whether a substantial number of small entities are, or are not, affected. Moreover, neither rule adequately explained why the impact of the rule would not be significant. The Food Safety and Inspection Service-USDA. The Food Safety and Inspection Service (FSIS) is a division within the U.S. Department of Agriculture. It issued "policy changes" at least twice in 1999 affecting thousands of small entities.(16) Despite the impact of both policy changes, the agency failed to do any economic analyses. In the opinion of the Office of Advocacy, this violated the Administrative Procedure Act, as FSIS failed to publish the changes as proposed rules. When rules are not published for public notice and comment they are not subject to the requirements of the RFA-resulting in further negative impacts on small business. On a positive note, FSIS contacted Advocacy in September 2000, requesting a tailored briefing on how to comply with the RFA. Advocacy conducted this briefing for about 25 FSIS and USDA staff, with great emphasis on the definition of a small entity for purposes of the RFA. Advocacy hopes the briefing will serve to make FSIS more sensitive to small business issues in the future. The Future Unresolved Issues on Which Reasonable People May Differ The RFA Imposes an Analytical Process on Regulatory Development-Not Just a Procedure As stated earlier, some agencies treat the RFA as though it is solely a procedural hurdle rather than an analytical process they must follow. Often these agencies craft their regulations and then devise analyses to justify the agencies' policies. Advocacy is of the view that the RFA requires agencies to make the analyses an integral part of regulatory development-while the rule is being drafted. Shortcuts frequently lead to folly, as illustrated by the following example in which the General Accounting Office (GAO) sanctioned a rule over Advocacy's objections, despite concluding that the data used in the rule were fatally flawed. The Food and Drug Administration (FDA) proposed a rule to regulate dietary supplements containing herbal ephedra (an herb that has properties similar to the chemical pseudoephedrine which is used in over-the-counter cold medications). In proposing the regulation, the agency cited thousands of adverse event reports (AERs) supposedly linked to the use of products containing herbal ephedra. The new dosage and labeling requirements in the proposal would mean that the product could no longer be marketed for weight loss. In reality the agency failed to provide a factual basis to support the need for the regulation. Further investigation by Advocacy and the industry revealed that hardly any of the AERs established a causal connection to the use of ephedra. If no causal connection is established, there is no basis for the rule. The GAO was asked by Congress to examine the scientific basis for FDA's proposed rule and examine FDA's adherence to the regulatory analysis requirements for federal rulemaking. In its report, Dietary Supplements: Uncertainties in Analyses Underlying FDA's Proposed Rule on Ephedrine Alkaloids (July 1999), the GAO found serious deficiencies with the data and studies used to support the regulation. The GAO stated that FDA did not establish a causal link between the ingestion of the products and the occurrence of adverse events for either its proposed dosing level or duration of use. FDA's benefits analysis could not be duplicated because it failed to identify which "serious" adverse event reports it had relied upon. The GAO also stated that FDA had no internal guidance on the use of AERs for rulemaking related to dietary supplements, and the AERs were used differently in this proposed rule than in prior rulemaking. Finally, the GAO indicated that the agency did not always disclose why certain key assumptions were made, the degree of uncertainty involved in those assumptions, or the fact that alternative assumptions would have had a dramatic effect on the agency's estimate of the benefits. After reaching these conclusions, the GAO inexplicably found that FDA met the requirements of the RFA. This conclusion, of course, is counterintuitive. How did the GAO reach this conclusion? The obvious answer: by treating the RFA as a mere procedural statute. According to the GAO, FDA jumped through all of the necessary RFA "hoops," so the fact that the data and analysis relied on by the FDA were flawed was irrelevant. The GAO explained that although the FDA acknowledged that the rule would affect small businesses, FDA adequately described the affected small businesses and discussed alternatives in compliance with the RFA. Perhaps the FDA concluded that since the RFA does not specifically require accurate data, then the RFA requirements were technically met-a preposterous theory. In Advocacy's view GAO's interpretation of the RFA's requirements is unquestionably erroneous and deviates completely from the purpose and intent of the RFA. GAO has issued similarly flawed reports in recent years that trend toward the agency treating the RFA as a procedural statute. Advocacy has serious concerns with GAO's conclusions about RFA compliance. In the future, GAO and other agencies must understand that the RFA imposes analytical as well as procedural requirements. What Did Congress Mean by "Significant" and "Substantial"? There has been much discussion over the years as to the need to define "significant" and "substantial" with some specificity. GAO is in the forefront of the effort to get specificity. Federal agencies believe that the undefined terms are too vague even though the nation has been well served by laws such as the Federal Trade Commission Act that outlaws "unfair competition" without defining "unfair competition." It is like pornography-one knows it when one sees it. When the RFA was adopted, Congress expressly left the terms undefined so that agencies would evaluate and analyze the impact of each regulation in the context of the industries being regulated and the types of requirements being imposed by the regulation. In other words, each regulation was to be treated as if it were the equivalent of a snowflake-each different in its own way. By not defining the terms, agencies could determine whether something was "significant" or "substantial" based on the unique requirements of the regulation and in the context of an ever-changing economy and changing industry structures. In the legislative history of the RFA, Congress discussed some of the measures an agency might use, but again, ultimately decided that definitive measures should not be included in the statute. For instance, legislative history says that the term "substantial" is intended to mean a substantial number of entities within a particular economic or other activity.(17) The history also states that agencies would not be required "to find that an overwhelming percentage [more than half] of small [entities] would be affected before requiring an IRFA."(18) As for "significant," Congress said, "the term `significant economic impact' is, of necessity, not an exact standard. Because of the diversity of both the community of small entities and of rules themselves, any more precise definition is virtually impossible and may be counterproductive."(19) Moreover, Congress identified several examples of "significant": a rule that provides a strong disincentive to seek capital;(20) having impacts greater than the $500 fine imposed for noncompliance;(21) new capital requirements beyond the reach of the entity;(22) any impact less cost-efficient than another reasonable regulatory alternative;(23) and any impact where the adverse cost impact is greater than the value of the regulatory good. Some agencies like the Marine Fisheries Service and the Department of Health and Human Services at some point established their own definitions for these terms. The latter has said that a rule is not significant if it would not reduce revenues or raise costs of any class of affected entities by more than three to five percent within five years. Advocacy believes it would be a daunting task to construct a specific definition or even a set of definitions that would apply to all industries for all times in an economy that is so diverse and in which the composition and cost and profit structures are constantly changing. No one can forecast how the economy will change, what industries will grow, what problems will emerge. Lack of specificity reserves the options for public policymakers to know "significant" and "substantial" when they see it and justify their analysis in the context of the economy as it exists when a rule is being developed. For these reasons, Advocacy is likely to discourage future attempts to construct a statutory or regulatory definition for these terms. Other Suggested Amendments to the RFA Other suggested amendments to the RFA would require agencies to weigh the indirect cost effects of regulation, and to close the loophole that allows agencies to bypass the requirements of the RFA by publishing interim or direct final rules. The future effectiveness of the RFA may be helped or hindered based on future amendments to the law. Budgetary Needs of Advocacy Advocacy does not have a line item in SBA's budget for a budget that includes salaries and expenses. Therefore, its budget and staffing are driven by SBA's support and budget constraints. The office can do as much or as little as the budget allows. Over the years, Advocacy's personnel ceiling has declined dramatically, despite increases in the statutory responsibilities undertaken by the office. Staff productivity has increased dramatically, due largely to an increase in the staff's expertise, as well as new working relationships with agencies and the regulated industries. Thus far, the staff has been able to avoid major omissions in its review of regulations, but the increase in resources being devoted to pre-proposal activity (over and above the SBREFA panel process) is stretching Advocacy's resources. There has been some congressional interest in giving Advocacy a separate line item in the SBA's budget for its entire operation but no action has been taken thus far.(24) Possible Legislative Proposals RFA Amendments. Since SBREFA became law in 1996, some observers have suggested further amendments to the RFA. For example, legislation introduced in the 106th Congress would have extended the SBREFA small business advocacy review panel requirements to the IRS and the Department of Labor's Mine Safety and Health Administration. Advocacy has not taken a position as to whether the addition of other agencies would be advisable, but does acknowledge that the process has worked well for the agencies that are currently covered by the panel requirements. Also, Advocacy encourages agencies to convene SBREFA-like panels on their own initiative since they are obligated under the RFA to reach out to small businesses in the development of regulations. Agency compliance with the outreach provisions of the RFA is subject to judicial review and instituting SBREFA-like panels could serve to satisfy an agency's obligations under the law. Advocacy's Independence. Two proposals were introduced that were designed to increase Advocacy's independence. One proposal would have established a separate budget line item for the office and defined the conditions under which the Chief Counsel could be removed. The second proposal would have created a three-member independent commission with rulemaking authority over compliance with the RFA and mandated a majority vote for all official commission actions (including comments submitted for the public record). Advocacy supported the first proposal, but had major concerns with the second. This is primarily because the second proposal would 1) take away Advocacy's ability to react quickly to fast-moving issues or emergencies; and 2) convert its work into litigious activities and thereby eliminate Advocacy's early access to policymakers in the executive branch.(25) No final action has been taken on either proposal. Conclusion The future is a difficult thing to predict. Should we believe Patrick Henry who once said, "I know no way of judging the future but by the past?" Or should we believe Edmund Burke who said, "You can never plan the future by the past?" Burke's theory seems more likely in light of these questions: Could anyone have predicted that after nearly 20 years of poor and/or spotty agency compliance with the RFA, some agencies would now be active partners with Advocacy in making better regulations that pose less of a burden on small entities? Could anyone have predicted that Advocacy, together with industry representatives, could save small entities billions of dollars annually by eliminating unnecessary and costly regulatory burdens? One thing is certain: hindsight has proven the RFA critics wrong. The RFA has been and will continue to be a valuable tool in the important work of fashioning fairer and better regulations. Moreover, agencies that have worked closely with Advocacy in recent years have found that RFA compliance does not necessarily impose increased cost or burden on the agency-particularly when the cost of litigation for noncompliance with the RFA is taken into consideration. "The Office of Advocacy's intervention in this matter is a valuable case study in the need for small businesses to have a federally established oversight organization to whom they can appeal in cases where agency impact analyses are seriously flawed."-Stephen F. Sims, Pharmaceutical Distributors Association, regarding Advocacy's comments on a rule issued by the Food & Drug Administration (FDA) Although it is impossible to know what the future holds, it can at least be said that the future looks promising. Each year since the passage of SBREFA, more and more agencies have made a good- faith effort to comply with the RFA-seeking RFA training, consulting with Advocacy early in a rule's development, etc. There is no reason for that trend to falter in the near future. Clearly, many agencies still need to do a better job and other agencies lack understanding of even basic RFA concepts. It is Advocacy's hope that all federal agencies will grow to appreciate the value and importance of the RFA. "FDA withdrew the most controversial portions of the proposed regulation . . . This is an astounding and unprecedented turnaround that would not have occurred without the SBA's help . . . As a result of the support the Office of Advocacy has provided, I am now convinced the SBA is an essential watchdog to prevent ill-conceived FDA regulations."-A. Wes Siegner, Jr., Hyman, Phelps & McNamara, P.C. In order for the regulatory environment to continue improving, the Office of Advocacy must be allowed to pursue its unique mission of representing small businesses within the federal government zealously and independently. Advocacy's ability to pursue its mission will hinge largely on two factors. The first is adequate funding from Congress. This will ensure proper staffing of the office and continued availability of vital economic research for policymakers. The best way to ensure proper funding may be to make Advocacy's budget a separate line item in the budget. Whatever the formula for Advocacy's funding in the future, the office will continue to utilize its resources to serve as the nation's watchdog against excessive government regulation. The other factor is the skill of the Chief Counsel to forge consensus between the executive and legislative branches of government and to open up policy councils to meaningful participation by small businesses. Credibility and nonpartisan relations with Congress, executive branch agencies and the small business community, as well as rapid responses to regulatory and policy initiatives, are key to effective representation of small business issues by a Chief Counsel. This is perhaps the single most important aspect in motivating the entire office, and it ensures the commitment of a team of professionals to small business. Appendix B: Fiscal Year 2000 Report on Agencies' Compliance with the Regulatory Flexibility Act Table of Contents Department of Agriculture Agricultural Marketing Service Food and Nutrition Service Food Safety and Inspection Service Forest Service Department of Commerce National Marine Fisheries Service Department of Health and Human Services Food and Drug Administration Health Care Financing Administration Department of the Interior Bureau of Land Management Fish and Wildlife Service Department of Labor Occupational Safety and Health Administration Department of Transportation Federal Aviation Administration Federal Motor Carrier Safety Administration Department of the Treasury Bureau of Alcohol, Tobacco and Firearms Internal Revenue Service Office of Thrift Supervision Environmental Protection Agency Federal Communications Commission Federal Reserve System Securities and Exchange Commission Federal Procurement Environmental Protection Agency Federal Acquisition Regulation Council Entities Not Covered by the RFA Internet Corporation for Assigned Names and Numbers United States Postal Service World Intellectual Property Organization Department of Agriculture The U.S. Department of Agriculture (USDA) was established in 1862 by President Lincoln. Since then, USDA has been charged with a very wide and diverse set of responsibilities such as farm support programs, soil conservation measures, feeding programs, inspection of meat and poultry, raising rural homeownership, research on pest management, biotechnology, nutrition and food safety, and management of 192 million acres of national forest and grasslands. Historically, USDA has demonstrated a spotty history of compliance with the Regulatory Flexibility Act (RFA). As described below, throughout fiscal year 2000, the Office of Advocacy continued to work with various agencies within USDA to improve their RFA compliance activities. In addition to the specific issues listed in this section, Advocacy has also commented on a number of other major USDA- proposed regulations. Since most of the work on these draft regulations contains confidential interagency work product, they cannot be discussed in detail herein. These proposed regulations included many important regulations, such as USDA's rule creating national standards for organic farming and processing. Agricultural Marketing Service In the early 1990s, Advocacy finally convinced the Agricultural Marketing Service (AMS) that its programs were subject to the RFA. Since the passage of the Small Business Regulatory Enforcement Fairness Act (SBREFA) in 1996, AMS has included more analysis in its regulations, frequently opting to prepare an initial regulatory flexibility analysis (IRFA) rather than certify their regulations. However, many of the analyses generally seem to miss a fundamental element: an explanation of why marketing orders and promotion programs are necessary and promote better economic results than a free-market scheme. This is an arcane area of law complicated by the fact that the regulated businesses frequently decide how they are to be regulated-that is, packing requirements, fruit size requirements, whether to adopt a promotion program, etc. The exception to the rule regarding AMS' track record of RFA compliance is the Organic Program Office. This unit within AMS has worked diligently with Advocacy and the Office of Management and Budget (OMB) for over two years to develop regulations for a national organic program. The Organic Program staff met with Advocacy very early in the rule's development in an attempt to make small business concerns an integral part of the rule. In terms of process and outcome, this approach is generally better than writing a rule and then figuring out how to fit small businesses into the equation. Food and Nutrition Service Issue: Food Stamp Retailer Eligibility. In June 1999, the Food and Nutrition Service (FNS) proposed a rule to revise the criteria for retail stores that wish to continue participating in the food stamp program. The primary purpose of the rule is to ensure that food stamp recipients continue to have adequate access to stores where they can purchase a wide variety of nutritious food items. FNS determined that a qualifying business must maintain no fewer than three different varieties of staple food items out of four statutorily defined categories, including perishable foods in at least two of those categories. For example, a retailer selling whole, skim, and chocolate milk can only claim one variety of dairy product. In order to ensure the sufficiency of stock on a continuing basis, FNS determined that a qualifying business must be able to verify at least $30,000 in wholesale purchases annually. These were deemed "Criterion A" requirements by the agency. If a business cannot meet "Criterion A" requirements, it can qualify for "Criterion B," which requires a business to have more than 50 percent of its total sales in staple foods. Although the agency certified under the RFA that the regulation would not have a significant economic impact on a substantial number of small entities, there was no factual basis for its certification. There was no mention of the number of small entities affected by the rule, which is the basic requirement for determining whether a substantial number of small entities were affected. There was no explanation for the seemingly arbitrary requirements in the rule, such as the $30,000 minimum in wholesale purchases, and why such a requirement would have no significant economic impact on small businesses. The intent of Congress when it mandated changes in the retailer eligibility requirements was to eliminate marginal stores that do not provide enough nutritious foods. Thus, Advocacy questioned whether there is any beneficial effect if stores covered by the rule are eliminated, even if they carry substantial amounts of staple foods. By not doing an economic analysis, the agency may also be harming the food stamp beneficiary if he or she has to travel further distances to find a store that does meet the criteria. Advocacy filed comments with FNS on August 27, 1999, urging the agency to re-propose the regulation with either a factual basis for its certification or an IRFA. Advocacy awaits further action from the agency on the rule. Issue: Vendor Participation Requirements for the Women, Infants, and Children Program. In June 1999, FNS published a rule that would strengthen requirements for operation of vendor management systems by limiting the number of vendors and imposing training requirements. As with the food stamp retailer rule above, the agency certified the regulation as having no significant impact on small businesses. Advocacy again asserted that there was no factual basis or data to support the certification. There was no discussion of the costs associated with limiting the number and distribution of authorized vendors that have never defrauded the government; or a description or estimate of the number of small entities that will be affected by the rule. Therefore, the rule has the potential of affecting not only abusive vendors, but legitimate vendors as well, based on whether participants have adequate access to the program. For example, if a large chain store is serving the area adequately, a smaller store might be eliminated from the program. Controversy swirled around a similar rule that was proposed by the FNS about eight years prior to the instant rule, so the agency needs to be particularly mindful of the rule's impact. Advocacy filed comments with FNS on August 27, 1999, voiced these concerns, and requested that the agency re-propose the regulation with a certification and adequate factual basis for the rule, or prepare an IRFA. To date there has been no response by FNS to Advocacy's request. Food Safety and Inspection Service The Food Safety and Inspection Service (FSIS) is another office within USDA that Advocacy believes still needs more work to improve RFA compliance. For example, FSIS issued "policy changes" at least twice in 1999 affecting thousands of small entities. One policy change eliminated face-to-face label reviews, and the other dealt with adding beef trimmings to the range of products that would be considered adulterated when contaminated with a particular food pathogen. The first of these two policy changes threatened to put many courier/expediter services out of business by not allowing meat processors to use couriers to meet in person with USDA label reviewers for instant label reviews. It also threatened to do great damage to the small processors who relied on courier services to obtain rapid approval on label changes. Ironically, elimination of the face-to-face process contravened USDA's own internal reports that hailed the process as successful and efficient. The second policy change was a sweeping expansion of FSIS policy interpretation of adulterated meat. Despite the impact of both "policy changes," the agency failed to do any economic analyses. In Advocacy's opinion, this violated the Administrative Procedure Act (APA) as FSIS failed to publish the changes as proposed rules. Moreover, when rules are not published for public notice and comment, they are not subject to the requirements of the RFA. Although the agency seems to have survived a court challenge in the case of the label reviews,(1b) the agency's resources probably would have been better utilized by issuing a proposed rule and preparing a proper analysis. In September 2000, FSIS contacted Advocacy requesting a tailored briefing on how to comply with the RFA. Advocacy conducted this briefing for about 25 FSIS and USDA staff, with great emphasis on the definition of a small entity for purposes of the RFA. Advocacy hopes the briefing will serve to make FSIS more sensitive to small business issues in the future. Forest Service The USDA's Forest Service is responsible for providing a continuing flow of natural resource goods and services to help meet the needs of the nation and to contribute to the needs of the international community. It is responsible for providing a sustained flow of renewable resources (outdoor recreation, forage, wood, water, wildlife, and fish) in a manner that best meets the needs of society now and in the future. FS is also responsible for assuring that nonrenewable resources are administered in a manner to help meet the country's needs for energy and minerals. With the exception of timber-related issues such as the spotted owl, Advocacy's interaction with FS was limited in the past. However, in fiscal year 2000, Advocacy became more active in FS' regulatory process. Issue: Limitation on Road Construction in National Forests. In October 1999, the administration directed FS to draft a rule to prohibit road construction and reconstruction in approximately 54 million acres of inventoried roadless areas. There was an exception in the rule for valid existing rights, public health and safety requirements, and conservation protection for threatened and endangered species. To meet the administration's directive, FS assembled an interagency team to assure compliance with various requirements of laws such as the National Environmental Policy Act (NEPA) and RFA. FS asked Advocacy to be a part of that interagency team, and Advocacy's primary role in the interagency effort was to advise the agency on RFA compliance. Initially it was FS' position that an RFA analysis was not necessary because the initiative would not have a significant impact on a substantial number of small entities. Advocacy believed that the proposal could have a foreseeable adverse impact on several small entities, including members of the timber industry, small natural-resource-dependent communities, members of the mining industry, recreation providers such as companies that rent snowmobiles and outfitters, and construction companies. Advocacy raised its concerns to FS verbally and in writing prior to the publication of the proposed rule in the Federal Register. Advocacy was concerned about the lack of information on the impact that the initiative would have on small businesses and communities, such as reduced revenues, increased costs, and dissolution of businesses due to the lack of access to natural resources found on federal lands. Although FS continued to contend that there was no direct significant economic impact, in the end, the agency heeded Advocacy's advice and prepared an economic analysis. Since FS did not have sufficient information to prepare a meaningful economic analysis, Advocacy asserted that FS had a duty to make a good- faith effort to obtain the data it needed to determine the economic impact of the proposed rule on a diverse group of small entities. Advocacy suggested that FS publish a list of questions along with the proposed rule in order to solicit the necessary information from the public. FS prepared such a list and published the proposed rule in May 2000. When the public comment period closed on July 17, 2000, FS had received thousands of comments on the proposal. Advocacy also filed comments, and acknowledged FS' cooperation in preparing a regulatory flexibility analysis. Advocacy also stressed the importance of FS giving full consideration to the information and the alternatives provided by the public in response to the IRFA. Currently, Advocacy is working with FS as it reviews the public comments and prepares the final rule, which is expected to be published in late December 2000. Department of Commerce The U.S. Department of Commerce (DOC) is responsible for encouraging the nation's economic growth, international trade, and technological advancements. A number of agencies within DOC are responsible for achieving this mandate. The agencies manage programs affecting diverse areas of commerce, such as fisheries, telecommunications, economic development, electronic commerce, and patents. National Marine Fisheries Service The fishing industry is dominated by small entities, and the economies of many small communities across the country are highly dependent on the fishing industry. Regulations that adversely affect the fishing industry also affect the fishing communities. The National Marine Fisheries Service (NMFS), a division of DOC's National Oceanic and Atmospheric Administration (NOAA), promulgates the majority of the regulations affecting small entities in the fishing industry. NMFS regulates the activities of small businesses under several natural resource protection statutes such as the Marine Mammal Protection Act and the Magnuson-Stevens Fishery Conservation and Management Act. NMFS promulgates rules through fishery councils located in different geographical parts of the country. Some councils have better information collection systems than do others. This affects the quality and consistency of the economic analyses performed by NMFS. The lack of consistent economic information has hindered NMFS' ability to perform thorough and credible economic analyses in compliance with the RFA. As an agency, NMFS has demonstrated a significant amount of improvement in its RFA compliance over the last few years. Advocacy believes that NFMS has made an institutional decision to comply with the RFA rather than circumvent its provisions. Historically, NFMS would certify that there was no significant impact on a substantial number of small businesses even if the certification was not supported by the data. Subsequent to the passage of SBREFA, NMFS' RFA compliance came under judicial and legislative attack. In response to pressure from the courts and Congress, NMFS hired an economist and an attorney specifically to address RFA compliance. NMFS also hired an ombudsman for small entity issues. In fiscal year 2000, the agency continued to make changes to its institutional framework in an attempt to advance its compliance with the RFA. A major change included new guidelines for review of impacts. NMFS completed its new agency guidelines to assist its regulators in performing economic analyses that comply with the RFA. The guidelines stress that a certification is the exception and should only be used in instances where the lack of an economic impact is clear. In all other instances, the regulators are directed to perform the necessary IRFA or final regulatory flexibility analysis (FRFA). NMFS is also working with its analysts to develop better alternatives to proposed rules and to gather the financial information that it needs to perform thorough economic analyses. Advocacy also holds regular issues "roundtables" attended by members of the fishing industry trade associations and officials from NMFS, NOAA, and DOC's Office of the General Counsel. At these meetings, fishing industry representatives have questioned whether NMFS is using the best available science in determining the appropriate manner to address fishery management. The best available science provides data on the status of the stock, which, in turn, determines which alternative(s) should be selected to address the particular management issue. Likewise, there are concerns about NMFS' failure to develop meaningful alternatives that allow for the survival of the fishery during the rebuilding period. Advocacy has raised these industry concerns with NMFS.(2b) Issue: Reduced Shark Quotas. On December 20, 1996, NMFS published a proposal to reduce the existing shark fishing quota by 50 percent and certified that the reduction would not have a significant impact on a substantial number of small entities. Thus began a lengthy saga of communications between Advocacy and NMFS, in which Advocacy maintained that NMFS had not complied with the RFA and that its economic analyses were significantly flawed.(3b) The industry sued NMFS on this issue. The case, Southern Offshore Fishing v. Daley,(4b) was eventually referred to a special master by the U.S. District Court for the Middle District of Florida after an unsatisfactory remand to the agency. On October 1, 1999, the special master submitted his findings and recommendations to the court. The special master held that: NMFS failed to collect meaningful economic data and this failure was arbitrary and capricious. Further, NMFS did not have all the necessary information to evaluate and implement alternatives to the quota. NMFS' failure to give any consideration to alternatives to the quota was a wanton repudiation of the court's instruction on remand. NMFS acted with a lack of good faith and contrary to the court's express instructions in the preparation of the remand submission. The special master concluded that NMFS' conduct constituted bad faith and a lack of candor to the court. The DOC filed objections to the special master's findings. In November 2000, federal regulators agreed to delay a decision on new shark fishing quotas until after a review of current and future shark stocks by a group of independent scientists. The decision for an independent review is part of a court settlement reached between the National Marine Fisheries Service and the Southern Offshore Fishing Association. The court still must approve the settlement agreement. Issue: Spiny Dogfish. On August 3, 1999, NMFS published a proposed Spiny Dogfish Fishery Management Plan. The intent of the plan was to rebuild the spawning fishing stock and eliminate overfishing while allowing for a one-year exit fishery. The average annual landings for the 10 years prior to the rule were 40 million pounds. The proposed plan implemented a commercial quota that allowed for 22 million pounds in year one and 2.9 to 3.2 million pounds for years two through five. NMFS prepared an IRFA for the proposal. In the proposal, NMFS acknowledged that: (1) in year one of the rebuilding schedule, there will be a 30 percent reduction in landings; (2) in the second year, there will be an 89 percent reduction in landings; and (3) the reduction in landings could result in the elimination of the remaining three dogfish processing plants and the total collapse of the U.S.-based markets for spiny dogfish harvesting and processing. Advocacy filed its comments on September 17, 1999, arguing that it was counterintuitive to implement a plan to rebuild a stock for a fishery that was being forced out of business by the implementation of the plan. Advocacy also criticized NMFS' failure to consider less restrictive alternatives, such as landing limits, size limits, seasonal closings, gear alternatives, and a fishery directed towards male dogfish. Advocacy argued that although NMFS stated that it considered 12 alternatives to the quota, they were actually variations of two themes: quotas and size limits. Advocacy compared the alternatives cited to the ones used by NMFS in the Southern Offshore Fishing case where the court characterized NMFS' treatment of alternatives as superficial. Advocacy also questioned whether NMFS met its obligations under National Standard 8 of the Magnuson Act, which requires NMFS to consider the importance of fishing resources to the fishing community and select the alternative that minimizes the impact. The New England Council and the Mid-Atlantic Council disagreed on the amount of the quota, and the issue was referred to the Secretary of Commerce. In April 2000, the rule became effective when the Secretary of Commerce issued an opinion that reduced the quota to 4.5 million pounds. The industry (fishers, processors, and dealers) filed suit in Massachusetts against DOC on February 8, 2000, and sought injunctive relief in May 2000, on the basis that the industry would cease operations under the allowable quota.(5b) In July 2000, the U.S. District Court upheld the Secretary of Commerce's decision on the basis that the action was necessary to sustain the fishery and for DOC to meet its obligations under the Magnuson Act. Department of Health and Human Services The U.S. Department of Health and Human Services (HHS) is the principal federal agency for protecting the health of all Americans and providing essential human services, especially for those who are least able to help themselves. HHS includes more than 300 programs that cover a wide spectrum of activities, such as medical and social science research, prevention of outbreak of infectious disease, food and drug safety, Medicare (health insurance for elderly and disabled Americans), Medicaid (health insurance for low-income people), and financial assistance for low-income families. In recent years, Advocacy has actively partnered with several branches of HHS to create a better regulatory environment for small entities. For instance, in March 1999, Advocacy held two in- depth training sessions for staff of its Health Care Financing Administration (HCFA) at the agency's headquarters in Baltimore. Those training sessions and several meetings with HCFA officials have led to a less contentious relationship between HCFA and Advocacy. This has in turn allowed Advocacy to have early input on several key regulations. Despite HCFA's challenging congressional mandate, Advocacy believes that the agency could do a better job of considering less burdensome regulatory alternatives that still meet statutory requirements. Many health care providers have expressed great frustration with HCFA and its regional carriers in particular. It is hoped that HCFA will rid itself of this negative public perception by looking more closely at regulatory alternatives and by forcing its regional carriers to apply HCFA's guidelines with significantly greater consistency. On the other hand, the Center for Food Safety and Applied Nutrition (CFSAN), within HHS' Food and Drug Administration (FDA), should be lauded for its efforts to help small entities. CFSAN has worked with Advocacy by offering briefings on upcoming regulations that will affect small entities before the regulations are even proposed. CFSAN seems to have made an institutional adjustment and a conscious decision to analyze the impact of their regulations on small entities thoroughly, thereby mitigating adverse impacts where possible. This institutional change at CFSAN came after several harsh comments from Advocacy that criticized the agency's analyses and its failure to comply with the RFA. Officials from CFSAN have stated that it is more productive to work with Advocacy in the earliest stages of rule promulgation than against Advocacy after a negative comment has been received. Certainly, more agencies should adopt this philosophy, including CFSAN's parent agency, HHS. CFSAN has also published a small business guide on writing effective comments to agency proposals. By following this basic guide, small businesses are able to write effective comments that explain the rule's impact on their business and provide invaluable data to the agency. Advocacy's relationship with other agencies within HHS is described below. In addition to the regulatory issues listed in this section, Advocacy has also commented on a number of other major HHS-proposed regulations. However, since most of the work on these regulations contains confidential interagency work product, they cannot be discussed in detail herein. Some of these regulations include a health information privacy rule that seeks to impose strict requirements on health care providers and their business partners regarding the handling of confidential information; HHS' rule on standards for electronic transactions in health care that governs confidentiality of electronic patient health records; and FDA's egg labeling and refrigeration rule to promote egg safety. Food and Drug Administration Issue: Disease Claims on Dietary Supplement Labels. This rule was highlighted in Advocacy's 1998 annual report, but it has since become final. In 1998, FDA published a proposed rule outlining, and defining, the types of statements that can be made concerning the effect of a dietary supplement on the structure or function of the human body. The rule also established criteria for determining when a statement about a dietary supplement is a prohibited disease claim. On October 14, 1998, Advocacy submitted comments regarding the proposed definition of "disease" and the negative impact such a definition would have on small businesses. Among other things, Advocacy proposed that FDA not expand the definition to include otherwise legal, truthful, and nonmisleading statements about the effects of a product on the normal structure or function of the body. In December 1999, both the OMB and FDA contacted Advocacy to review and comment on the draft final rule. When the final rule was published on January 6, 2000, the provisions that were most harmful to small businesses had been modified. FDA redefined "disease" to comport with the previous statutory definition. References to journal articles/titles will be permitted on product labeling. In addition, statements that apply to conditions associated with natural states or processes like pregnancy or aging will also be allowed. Finally, more acceptable data on the number of affected small entities was utilized, which resulted in a more accurate impact analysis of the rule. Issue: Drug Pedigree Requirements. The Prescription Drug Marketing Act (PDMA) was created to combat abuses involved in the distribution of prescription drugs. It contains drug pedigree requirements that impose prior sale documentation obligations on nonauthorized distributors. Central to whether a business would have to comply with the documentation requirements is whether a business is "an authorized distributor of record" that maintained an "ongoing relationship" to distribute a manufacturer's products. Guidance issued by FDA in 1988 stated that "ongoing relationship" was to be interpreted broadly, and that the existence of two transactions in a two-year period would be presumptive evidence of a continuing relationship. The 1992 PDMA amendments altered the information requirements that had to be provided prior to each wholesale distribution of a drug. When FDA proposed its regulations to implement the PDMA amendments on March 14, 1994, it instituted a sudden reversal of policy. The regulations changed the definition of "ongoing relationship" to make it harder to become an authorized distributor. It gave manufacturers the sole discretion to determine who should be designated as an "authorized distributor." The proposal required a written statement between a manufacturer and each authorized distributor, and each distributor must appear on the manufacturer's list of authorized distributors. The industry requested that FDA revise the rule to require that the pedigree go back only as far as the last authorized distributor of record, and not for each one in the chain. When the final rule was published on December 3, 1999, it was obvious that FDA rejected the industry's request. Advocacy submitted comments to FDA on February 29, 2000, petitioning the agency (pursuant to section 553 of the APA) to reconsider the final rule, suspend the effective date, and reissue regulations that will carry out the intent of Congress with respect to the PDMA. Advocacy argued that FDA's regulatory scheme ignored the reality of the relationship between secondary drug wholesalers and manufacturers. Manufacturers can choose to limit those businesses that they consider authorized distributors. Also, drug products currently in the inventory of wholesalers would have to be cleared out and new orders would have to cease, or be severely limited, within one year to accommodate the actual effective date of the rule. Moreover, secondary wholesalers (who buy from full- line wholesalers that do not provide a pedigree) would not be able to provide a pedigree to their customers describing transactional information back to the manufacturers. On May 3, 2000, a delay of the effective date of the proposed rule was announced in the Federal Register. Affected entities will not have to comply until October 2001, pending further study and analysis of the rule. Issue: Pre-Market Approval for Silicone Breast Implants. Advocacy began working on this issue in 1999 when FDA published a final rule designating the effective date for requiring the filing of a pre-market approval application (PMA) or a notice of completion of product development protocol (PDP) for silicone inflatable breast prostheses. The regulation would require commercial distribution of the device to cease unless a manufacturer, or importer, filed a PMA or PDP within 90 days of the effective date. FDA estimated that the cost of compliance with the rule would be $1 million per PMA, and certified that there would not be a significant impact on small businesses because the industry was aware that PMAs were inevitable. Advocacy filed comments on September 9, 1999, saying that FDA failed to provide a factual basis for their certification. There were no estimates of the number of small entities affected and no information on why the $1 million estimate per PMA was not a significant cost for businesses to bear. Advocacy requested that FDA republish the rule with a proper certification. In a November 16, 1999, letter to Advocacy, FDA claimed that only seven entities would be affected. According to the FDA, five of the entities were large and/or foreign businesses, and they were already legally marketing the products. FDA claimed that the two remaining companies did not constitute a "substantial number of small entities" per the RFA. In short, the agency declined to republish the rule. Advocacy submitted additional comments to the FDA on February 9, 2000, stating that the two businesses do in fact constitute a substantial number for the purposes of the RFA because those two businesses constituted 100 percent of regulated small entities. The letter also alluded to a disturbing pattern whereby FDA assumed a similar position regarding the interpretation of "substantial number" in another rule concerning ophthalmic eye shields. No further comment has been received from the FDA to date. Issue: Sterility Requirements for Aqueous-Based Drug Inhalation Products. FDA proposed a regulation that would raise the number of inhalation solution products manufactured with a sterile process from 50 percent to 100 percent in order to reduce the incidence of adverse drug reactions from contaminated nonsterile solutions. FDA identified five firms (representing 18 percent of the regulated industry and 100 percent of small businesses) that did not use a sterile process or that contract out the process. FDA stated that the five firms could expect to incur costs from $270,000 to $1.7 million each. Advocacy filed comments on December 18, 1997, that criticized the lack of estimates for training and paperwork, the lack of data on illnesses caused by nonsterile products and the lack of less burdensome alternatives. Advocacy requested lengthening the compliance date from one year to two and end testing products for signs of contamination rather than requiring a sterile process. On February 7, 2000, FDA sent Advocacy a copy of the draft final rule for review. The rule reflected a sizeable reduction in the small business burden. The scope of the regulation was clarified to limit the rule's applicability, and the time for compliance was increased to two years. For the first time, the regulation contained data on actual adverse event reports associated with nonsterile products that had occurred in the past. The one-year delay resulted in a one-time saving to small businesses of $10.1 million. Health Care Financing Administration Issue: Medicare Ambulance Fee Schedule. This rule was highlighted in Advocacy's 1998 annual report, but it has since become final. In 1997, HCFA proposed a regulation to reduce Medicare costs resulting from the use of ambulances where no medical necessity existed, or where reduced services may suffice. HCFA proposed to base Medicare reimbursement on the beneficiary's medical condition rather than the type of vehicle used. The rule would have required ambulance services to document and submit to HCFA a record of the level of medical care needed by a beneficiary, based on certain limited and pre-determined codes. The rule also proposed to narrow the definition of an ambulance by requiring a certain number of personnel to operate each vehicle and certain minimum supply and equipment levels. Based on Advocacy's November 4, 1997, comments, as well as other comments filed by industry, HCFA published a final rule in 1999 that modified certain portions of the proposal. More important, HCFA called for a negotiated rulemaking to decide the proper definition of the various classes of ambulances. The 1999 rule reduced the equipment requirements, modified staff requirements to comport with state laws, and removed physician certification requirements in certain circumstances. On September 12, 2000, the agency published its proposed Medicare ambulance fee schedule, which drew heavily from a fee schedule negotiated with industry groups. For example, most of the cost shifting will come from urban areas and go to rural areas (which incur higher costs per trip). There will be seven categories of ground ambulance services rather than two. There will be a set reimbursement rate for each category, based on the relative cost of the service, adjusted for wage differences. As a result of these provisions rural areas will receive higher reimbursements for the service. HCFA proposes to phase in the revised schedule over four years. As a result of the negotiated rulemaking, the fairness of the rule has been enhanced. Issue: Competitive Bidding Demonstration Projects for Durable Medical Equipment. As described in Advocacy's 1998 and 1999 annual reports, this program seeks to limit the number of providers in a designated region for selected types of durable medical equipment and home medical equipment supplies. Under the demonstration, only successful bidders will be able to participate in the Medicare reimbursement program. Advocacy commented about the program twice, once to HCFA on November 11, 1998, and once to OMB on December 18, 1998. Meetings were held at OMB to negotiate the details of the regulation. Aside from the burden imposed by the bidding requirements, the biggest problem was that HCFA saw no need to publish a proposed rule. It chose instead to publish a direct final rule. Additional issues were raised during the OMB meetings, such as the program's compatibility with the agency's proposal on consolidated billing for skilled nursing facilities, and whether sensitive financial data should be collected from prospective bidders that were not finalists. HCFA redesigned some portions of the bid packages based on concerns voiced by Advocacy and industry. Even after the changes, the agency acknowledged that reimbursement to winning suppliers would be reduced by 13 to 31 percent. During August and September of 1999, HCFA apprised Advocacy of the preliminary results of the demonstration. It showed that 14 of the 16 winning suppliers were small entities. In October 1999, HCFA held a public meeting on a second demonstration project to be implemented in a different region of the country. The meeting allowed interested parties to furnish information and raise issues about the items selected for the demonstration, including the proposed site and quality standards for bidders. This marked a significant improvement over the manner in which the first demonstration was conducted because public input occurred before the rule reached the OMB review stage. In January 2000, HCFA officially proposed its second demonstration project, but again, the agency requested emergency OMB clearance for the bidding forms. Advocacy submitted comments to HCFA on February 14, 2000, criticizing the agency for seeking emergency clearance. The agency responded by indicating that it had to fit in all five demonstrations before its authorization expired in 2002. Advocacy argued in the alternative that the agency was permitted, but not required, to establish five demonstrations; therefore, emergency clearance should not have been sought. Advocacy also opined that some of the selected items (e.g., oxygen and wheelchairs) were not properly included in the items subject to bidding because of the heavy service component required for those items. Some small businesses have built a niche market for durable medical equipment that requires special orders or a heavy service component. No significant changes were made to the proposal by HCFA. Advocacy will actively continue to monitor future demonstrations. Issue: Prospective Payment System for Home Health Agencies. Advocacy was very involved in the predecessor to this rule, the interim payment system (IPS) for home health agencies (HHAs). That rule attempted to curb Medicare spending, fraud, and abuse by changing its reimbursement policy from one based on reasonable or actual costs to one based on caps. The caps were determined by analyzing historical costs for some agencies, and national average costs for other agencies. The regulation unfairly penalized historically low-cost HHAs, by giving high-cost agencies higher payments in most cases. Several unsuccessful lawsuits were filed by industry across the country. Industry relied on Advocacy's initial IPS comments to support their respective cases to argue that the IPS regulation violated the RFA. However, the court in Greater Dallas Health Care Alliance v. Shalala,(6b) concluded that HCFA did not violate the RFA and was simply doing what Congress mandated. Further history of Advocacy's involvement in IPS can be found in Advocacy's 1998 annual report. The prospective payment system (PPS) was required by the Balanced Budget Act of 1997, and was later refined by the Balanced Budget Refinement Act of 1999, and other laws. PPS was intended to replace the IPS with a more fair-minded approach to reimbursement. In the summer of 1999, HCFA requested Advocacy's comments on the draft proposed rule for PPS. Advocacy submitted its comments on August 26, 1999. On October 21, 1999, Advocacy was briefed by HCFA officials on the content of the PPS draft proposed rule and later briefed on the draft final rule on June 23, 2000. In reviewing the rules, Advocacy found that PPS was preferable to IPS because, among other changes, PPS will take into account the patient mix of an agency and allow for a change-in-condition adjustment if a patient's condition worsens. PPS will also allow for a restart of the 60-day episode if a patient is transferred to a different agency, and will delay for one year the 15 percent across-the-board reduction in payments (pursuant to the Balanced Budget Refinement Act). A town hall meeting was held by HCFA to explain the requirements of the rule shortly after publication of the final rule. The overall effect of the PPS rule will be to reduce some of the burden associated with IPS. Issue: Hospital Outpatient Prospective Payment System. This rule was highlighted in Advocacy's 1999 annual report. Like the home health care PPS, the hospital outpatient rule sought to change the system of Medicare reimbursement from one that was cost-based to one that is based on predetermined rates for individual services. Advocacy submitted comments to HCFA on July 29, 1999, suggesting that the agency should exclude cancer, rehabilitation, and rural or low-volume hospitals from the rule because they are highly specialized facilities and use advanced treatment modalities. For instance, the national median hospital costs proposed by HCFA did not support the sophisticated and evolving types of treatment in cancer hospitals. The proposal would have reduced payments to low- volume, cancer, and rehabilitation hospitals by 17.0, 29.2, and 24.1 percent, respectively. On November 29, 1999, the Administration signed the Balanced Budget Refinement Act of 1999, resulting in a 10 percent increase in payments to hospitals, and other additional payments to help hospitals make the transition from the cost-based system. Several specialty hospitals were excluded from the requirements of the outpatient rule. These change