99-23811. Agency Information Collection Activities; Submission for OMB Review; Comment Request; Collection of Letters of Interest and Food Safety Data in a Voluntary Pilot Program Using HACCP Principles for Retail Food Operations  

  • [Federal Register Volume 64, Number 177 (Tuesday, September 14, 1999)]
    [Notices]
    [Pages 49812-49814]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 99-23811]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    [Docket No. 98N-0572]
    
    
    Agency Information Collection Activities; Submission for OMB 
    Review; Comment Request; Collection of Letters of Interest and Food 
    Safety Data in a Voluntary Pilot Program Using HACCP Principles for 
    Retail Food Operations
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Notice.
    
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    SUMMARY: The Food and Drug Administration (FDA) is announcing that the 
    proposed collection of information listed below has been submitted to 
    the Office of Management and Budget (OMB) for review and clearance 
    under the Paperwork Reduction Act of 1995 (the PRA).
    
    DATES: Submit written comments on the collection of information by 
    October 14, 1999.
    
    ADDRESSES: Submit written comments on the collection of information to 
    the Office of Information and Regulatory Affairs, OMB, New Executive 
    Office Bldg., 725 17th St. NW., rm. 10235, Washington, DC 20503, Attn: 
    Desk Officer for FDA.
    
    FOR FURTHER INFORMATION CONTACT: Peggy Schlosburg, Office of 
    Information Resources Management (HFA-250), Food and Drug 
    Administration, 5600 Fishers Lane, Rockville, MD 20857, 301-827-1223.
    
    SUPPLEMENTARY INFORMATION: In compliance with section 3507 of the PRA 
    (44 U.S.C. 3507), FDA has submitted the following proposed collection 
    of information to OMB for review and clearance.
    
    Collection of Letters of Interest and Food Safety Data in a 
    Voluntary Pilot Program Using HACCP Principles for Retail Food 
    Operations
    
         Section 402 of the Federal Food, Drug, and Cosmetic Act (the act) 
    (21 U.S.C. 342) enables FDA to regulate the safety of foods in 
    interstate commerce. In addition, under authority granted in the Public 
    Health Service Act (the PHS Act) (42 U.S.C. 241, 243, and 264), the 
    agency engages in a range of activities intended to ensure the safety 
    of the nation's food supply, from regulating food when it can be a 
    vector of disease to assisting, and cooperating with, the States to 
    ensure effective State and local food safety programs. FDA endeavors to 
    assist the more than 3,000 Federal, tribal, State, and local regulatory 
    agencies that have primary responsibility for monitoring retail food 
    establishments to ensure that consumers are protected.
        FDA is proposing to collect information, through a voluntary pilot 
    program, on how hazard analysis critical control points (HACCP) 
    principles might be implemented in the retail food industry. The pilot 
    program is designed to provide insight into the problems, costs, and 
    benefits of developing and implementing HACCP principles for food 
    service, retail food stores, and other retail food establishments, in 
    order to improve and provide direct guidance to both the retail 
    industry and regulatory authorities for the implementation of HACCP 
    principles in the retail food sector. FDA will select candidates with a 
    goal of ensuring that the participants in the program cross the 
    spectrum of retail activities, have a range of scientific capabilities, 
    have facilities of varying sizes, and have a range of HACCP experience. 
    FDA has been approached by State and local governments to provide 
    guidance for applying HACCP principles at retail; therefore, the agency 
    intends to collect information through the pilot program to develop and 
    enhance guidance. The agency intends to make a summary of the results 
    of the retail pilot program publicly available.
         The agency will request retail food establishments and regulatory 
    agencies interested in participating in the pilot program to send to 
    FDA a letter of interest. Letters from regulatory agencies need only 
    state an interest in participating. FDA requests that the letters of 
    interest from retail food establishments describe their menu, the 
    location and size of their facility, the type of techniques they use to 
    prepare their products, and the extent to which, and how, they employ 
    HACCP; identify area government officials with whom they have worked to 
    implement or reinforce the system; identify which State, local, and/or 
    tribal government officials they would like to work with in the pilot 
    program; and identify trade associations they would like to work with 
    in the pilot. FDA will review the letters of interest from retail 
    applicants and identify a limited number of individual establishments 
    that represent a broad spectrum of the retail food industry and that, 
    in the judgment of the agency, are best suited to participate in the 
    pilot program. The retail pilot participants will maintain a food 
    safety program based upon HACCP principles for the duration of the 
    pilot. FDA will study the information and data the pilot participants 
    use to maintain their food safety programs.
         In the Federal Register of July 30, 1998 (63 FR 40716), the agency 
    requested comments on the proposed collection of information. The 
    agency received one comment from a trade association that represents 
    one segment of the retail food industry. The comment recommended that 
    FDA not pursue the pilot program as currently planned. Instead, the 
    comments suggested that the agency solicit industry and academic input 
    into the development of a ``new, more inclusive'' HACCP pilot program. 
    The comment's recommendation was based on several concerns.
    
    [[Page 49813]]
    
        First, the comment expressed concern that a mandatory information 
    collection regulation may mark the end of cooperative industry 
    development of HACCP programs.
        The voluntary retail HACCP pilot program is neither mandatory, nor 
    is it a regulation. The purpose of the pilot program is to enhance 
    understanding and implementation of HACCP principles through 
    cooperation among industry, FDA, and participating State and local 
    regulatory authorities. Any participant may leave the program at any 
    time. The agency hopes that the pilot will promote rather than curtail 
    the cooperative efforts toward building HACCP into retail. The agency 
    agrees with the statement in the comment that ``There are many problems 
    to overcome before HACCP can be fully implemented in the retail 
    industry and clearly cooperation and inclusion will provide the answers 
    to those problems.'' This is exactly why industry is being invited to 
    participate; the agency recognizes that industry involvement is 
    critical to furthering a cooperative relationship.
        Second, the comment expressed concern about the disclosure of 
    proprietary information and cautioned that access to voluntary HACCP 
    plans, including records and customer complaints, must be restricted. 
    The comment also stressed that the records must remain the property of 
    the establishment.
        The information collected at individual establishments will be held 
    as proprietary, and contracts are to be signed by all parties involved 
    limiting the use of the proprietary information. The agency intends to 
    review the systems implemented by the retail establishment, including 
    records, in order to document how the system works, but the records 
    will remain the property of the establishment. After the pilot, the 
    data collected at individual establishments will be generalized, and a 
    collective retail HACCP pilot report will be publicly disseminated. The 
    names and locations of the participating firms will be held as 
    proprietary unless authorized for release by the participant.
        Third, the comment raised several issues relating to consultation, 
    participation, and fairness. The comment expressed concern that FDA is 
    duplicating efforts by the restaurant industry and asserted that FDA 
    has not consulted with developers of existing HACCP programs or 
    evaluated these ongoing programs. The comment also charged that FDA 
    intends to exclude universities and trade associations from direct 
    participation in the pilot to prevent them from having input into any 
    final recommendations resulting from the pilot. More generally, the 
    comment expressed the view that FDA lacks the knowledge and detachment 
    to select participants in the pilot on an objective basis.
        The agency believes these concerns are unfounded. FDA intends to 
    build on retail industry efforts through the retail HACCP pilot program 
    by studying ongoing HACCP systems and documenting activities used by 
    the retail industry to fully implement a HACCP system. During the 
    design of the program, industry representatives shared their views on 
    how an effective pilot program should proceed and provided feedback and 
    guidance on this effort of collecting information. This information was 
    used in designing the retail HACCP pilot program.
        With regard to selection of participants, the design and intent of 
    the pilot is inclusive, not exclusionary. The pilot seeks to include 
    establishments that represent a broad spectrum of retail activities, 
    geographic locations, sizes, and levels of experience with HACCP. Since 
    each participant has the right, within the limits of the law, to 
    control access to its proprietary information, each participant has the 
    right to invite entities such as State, local, and tribal regulatory 
    agencies, universities, and trade associations to work with it during 
    the pilot, and it also has the right not to work with any such entities 
    (although participants will, of course continue to be subject to 
    applicable food safety laws and regulations in all jurisdictions during 
    the pilot).
         FDA will involve the pilot participants in the summary of results 
    and formation of conclusions at the end of the pilot program, and will 
    make the summary report publicly available. The pilot is designed to 
    encourage voluntary evolution of retail HACCP plans with the 
    involvement of all stakeholders: Government, industry, academia, and 
    trade associations.
        Fourth, the comment expressed doubts about the need for the pilot 
    program. The comment stated that the retail food industry has used 
    HACCP for many years with great success. According to the comment, FDA 
    should remain only an evaluator of the success of HACCP programs, and 
    should not attempt to institute or mandate such programs.
        FDA disagrees with the comment. The PHS Act provides that the 
    agency shall assist States and political subdivisions in the prevention 
    and suppression of communicable diseases, and with respect to other 
    public health matters, shall cooperate with and aid State and local 
    authorities in the enforcement of their health regulations, and shall 
    advise the States on matters relating to the preservation and 
    improvement of the public health. FDA is also entrusted with regulating 
    food safety under the act. Therefore, the agency is responsible for 
    carrying out these functions and intends to do so. The retail HACCP 
    pilot program is one of many elements necessary to enable FDA to 
    perform these statutory responsibilities.
        Fifth, the comment expressed concern about the recordkeeping 
    burdens that the retail HACCP pilot program would create for 
    participants. The comment asserted that massive recordkeeping paperwork 
    for the hundreds of items on restaurant menus would be required. The 
    comment expressed hope that the pilot does not move to apply a single, 
    ``one-size-fits-all'' FDA recordkeeping system.
        The agency is seeking information through the pilot program on the 
    amount and extent of recordkeeping that retail establishments have 
    determined necessary to effectively implement and manage their HACCP 
    systems. To be part of the voluntary pilot, the only recordkeeping 
    requirement is a letter to FDA expressing interest to participate in 
    the pilot program. The agency will not determine the amount or type of 
    records needed during the pilot; rather, each industry participant will 
    determine the amount and type of records it needs to effectively verify 
    that its system is working. Thus, the pilot program will not create an 
    undue burden and will not impose a single recordkeeping system on all 
    establishments.
        The comment also expressed the belief that FDA's burden estimate 
    did not account for all the time that would be required by the smallest 
    participants in this program to learn about and institute a HACCP 
    program. The comment further stated that FDA has not shown a 
    willingness to encourage or assist vital small restaurant operator 
    participation in this pilot.
        The agency will select candidates with a goal of ensuring that the 
    participants in the program cross the spectrum of retail activities, 
    have a range of scientific capabilities, have facilities of varying 
    sizes, and have a range of HACCP experience. The pilot program will 
    encompass the challenges unique to the retail environment, such as 
    multiple menu items, size of the facility, and employee turnover. The 
    agency intends to work with establishments with preexisting HACCP 
    programs and those establishments intending to start designing their 
    HACCP systems. The agency is seeking information that will document the 
    costs and time necessary for developing and implementing a HACCP 
    system.
    
    [[Page 49814]]
    
     FDA will also provide guidance and counseling upon request to those 
    participating establishments that are in the process of developing 
    HACCP systems, although the agency will not write HACCP plans.
        Finally, the comment expressed concern that agencies could make use 
    of prior establishment records as the basis for enforcement action.
        In order to deal with this concern, the agency intends to provide 
    clear direction to the pilot site teams to separate HACCP activities, 
    such as the establishment's performance of corrective action, from 
    system failures when risk factors are uncontrolled and enforcement 
    action may be necessary. FDA has initiated and intends to further train 
    the pilot site teams on how to evaluate a HACCP system and identify 
    items that are important. The establishment has the primary 
    responsibility to ensure the food is safe by fully implementing its 
    HACCP system, and the pilot site teams will evaluate the effectiveness 
    of that program.
        FDA estimates the burdens of this collection of information as 
    follows:
    
                                     Table 1.--Estimated Annual Reporting Burden \1\
    ----------------------------------------------------------------------------------------------------------------
                                                          Annual
                Activity                  No. of       Frequency per   Total Annual      Hours per      Total Hours
                                        Respondents      Response        Responses       Response
    ----------------------------------------------------------------------------------------------------------------
    Letters of interest from State/        50               1              50               1              50
     local/tribal authorities \2\
    Letters from interested retail         50               1              50               1              50
     firms \2\
    Total                                                                                                 100
    ----------------------------------------------------------------------------------------------------------------
    \1\ There are no capital costs or operating and maintenance costs associated with this collection of
      information.
    \2\ One time activity.
    
    
                                   Table 2.--Estimated Annual Recordkeeping Burden \1\
    ----------------------------------------------------------------------------------------------------------------
                                                          Annual
                Activity                  No. of       Frequency per   Total Annual      Hours per      Total Hours
                                       Recordkeepers   Recordkeeping      Records         Record
    ----------------------------------------------------------------------------------------------------------------
    Plan development                       40               1              40             100           4,000
    Plan implementation documents          40           7,000         280,000                .05       14,000
    Implementation review                  40               4             160               4             640
    Total                                                                                              18,640
    ----------------------------------------------------------------------------------------------------------------
    \1\ There are no capital costs or operating and maintenance costs associated with this collection of
      information.
    
        These estimates are based on FDA's experience with other pilot 
    programs and on comments received through the Conference for Food 
    Protection, public meetings, and through retail industry advice. This 
    information was utilized to design the pilot program with the least 
    amount of burden to the retail industry.
        Because only one letter of interest need be submitted per 
    prospective participant in the pilot, submitting the letter will create 
    only a minimal one time burden. Once the pilot program begins, FDA 
    estimates that the burden of collecting and maintaining food safety 
    information based upon HACCP principles will vary considerably across 
    the wide spectrum of retail activities and establishments, the types, 
    and numbers of products involved, and the nature of the equipment or 
    instruments required by the retail establishment for monitoring. The 
    recordkeeping burden to each retail participant would involve 
    maintaining a food safety plan based upon HACCP principles, generating 
    the necessary records to implement that plan, and checking the records 
    to verify implementation. Those participants who do not already have a 
    HACCP plan in place would also have to develop such a plan.
        Since the publication of the July 1998 Federal Register notice 
    seeking comment on the pilot program, FDA has learned from 
    conversations with potential participants that approximately 20 percent 
    of these potential participants are already using HACCP plans in the 
    normal course of their business activities. The PRA regulations (5 CFR 
    1320.3(b)(2)) provide that the time, effort, and financial resources 
    that would be incurred by persons in the normal course of usual and 
    customary activities are excluded from the burden of a collection of 
    information. Therefore, the agency has revised its estimates to reflect 
    the fact that the pilot program would impose no additional 
    recordkeeping burden on the establishments that are already using 
    HACCP.
    
        Dated: September 8, 1999.
    Margaret M. Dotzel,
    Acting Associate Commissioner for Policy.
    [FR Doc. 99-23811 Filed 9-13-99; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
09/14/1999
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice.
Document Number:
99-23811
Dates:
Submit written comments on the collection of information by October 14, 1999.
Pages:
49812-49814 (3 pages)
Docket Numbers:
Docket No. 98N-0572
PDF File:
99-23811.pdf