98-17601. Request for Nominations for Nonvoting Representatives of Consumer and Industry Interests on Public Advisory Panels or Committees  

  • [Federal Register Volume 63, Number 127 (Thursday, July 2, 1998)]
    [Notices]
    [Pages 36242-36244]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 98-17601]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    
    
    Request for Nominations for Nonvoting Representatives of Consumer 
    and Industry Interests on Public Advisory Panels or Committees
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Notice.
    
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    SUMMARY: The Food and Drug Administration (FDA) is requesting 
    nominations for nonvoting consumer representatives and nonvoting 
    industry representatives to serve on certain device panels of the 
    Medical Devices Advisory Committee in the Center for Devices and 
    Radiological Health (CDRH). Nominations will be accepted for current 
    vacancies and for those that will or may occur through June 30, 1999.
        FDA has a special interest in ensuring that women, minority groups, 
    individuals with disabilities, and small businesses are adequately 
    represented on advisory committees and, therefore,
    
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    encourages nominations for appropriately qualified candidates from 
    these groups, as well as nominations from small businesses that 
    manufacture medical devices subject to the regulations.
    
    DATES: Nominations should be received by (insert date 30 days after 
    date of publication in the Federal Register), for vacancies listed in 
    this notice.
    
    ADDRESSES: All nominations and curricula vitae for consumer 
    representatives should be submitted in writing to Annette J. Funn 
    (address below). All nominations and curricula vitae (which includes 
    nominee's office address and telephone number) for industry 
    representatives should be submitted in writing to Kathleen L. Walker 
    (address below).
    
    FOR FURTHER INFORMATION CONTACT:
        Regarding consumer representatives: Annette Funn, Office of 
    Consumer Affairs (HFE-88), Food and Drug Administration, 5600 Fishers 
    Lane, Rockville, MD 20857, 301-827-5006.
        Regarding industry representatives: Kathleen L. Walker, Office of 
    Systems and Management (HFZ-17), CDRH, Food and Drug Administration, 
    2098 Gaither Rd., Rockville, MD 20850, 301-594-1283, ext. 114.
    
    SUPPLEMENTARY INFORMATION: FDA is requesting nominations for nonvoting 
    members representing consumer and industry interests for the vacancies 
    listed below:
    
                                                                                                                    
    ----------------------------------------------------------------------------------------------------------------
                                                                               Approximate Date Representative is   
                                                                                             Needed                 
                             Medical Devices Panels                        -----------------------------------------
                                                                                  Consumer             Industry     
    ----------------------------------------------------------------------------------------------------------------
    Circulatory System Devices Panel                                        July 1, 1999.......   NV                
    Immunology Devices Panel                                                March 1, 1999......   NV                
    Obstetrics and Gynecology Devices Panel                                 NV.................  February 1, 1999   
    ----------------------------------------------------------------------------------------------------------------
    NV = No vacancy                                                                                                 
    
    Function
    
        The functions of the medical device panels are to: (1) Review and 
    evaluate data on the safety and effectiveness of marketed and 
    investigational devices and make recommendations for their regulation; 
    (2) advise the Commissioner of Food and Drugs regarding recommended 
    classification or reclassification of these devices into one of three 
    regulatory categories; (3) advise on any possible risks to health 
    associated with the use of devices; (4) advise on formulation of 
    product development protocols; (5) review premarket approval 
    applications for medical devices; (6) review guidelines and guidance 
    documents; (7) recommend exemption to certain devices from the 
    application of portions of the Federal Food, Drug, and Cosmetic Act; 
    (8) advise on the necessity to ban a device; (9) respond to requests 
    from the agency to review and make recommendations on specific issues 
    or problems concerning the safety and effectiveness of devices; and 
    (10) make recommendations on the quality in the design of clinical 
    studies regarding the safety and effectiveness of marketed and 
    investigational devices.
    
    Consumer and Industry Representation
    
        Section 520(f)(3) of the Federal Food, Drug, and Cosmetic Act (the 
    act) (21 U.S.C. 360j(f)(3)), as amended by the Medical Device 
    Amendments of 1976, provides that each medical device panel include as 
    members one nonvoting representative of consumer interests and one 
    nonvoting representative of interests of the medical device 
    manufacturing industry.
    
    Nomination Procedures
    
    Consumer Representatives
    
        Any interested person may nominate one or more qualified persons as 
    a member of a particular advisory committee or panel to represent 
    consumer interests as identified in this notice. Self-nominations are 
    also accepted. To be eligible for selection, the applicant's experience 
    and/or education will be evaluated against Federal civil service 
    criteria for the position to which the person will be appointed.
        Nominations shall include a complete curriculum vitae of each 
    nominee and shall state that the nominee is aware of the nomination, is 
    willing to serve as a member, and appears to have no conflict of 
    interest that would preclude membership. FDA will ask the potential 
    candidates to provide detailed information concerning such matters as 
    financial holdings, employment, and research grants and/or contracts to 
    permit evaluation of possible sources of conflict of interest. The 
    nomination should state whether the nominee is interested only in a 
    particular advisory committee or panel or in any advisory committee or 
    panel. The term of office is up to 4 years, depending on the 
    appointment date.
    
    Industry Representatives
    
        Any organization in the medical device manufacturing industry 
    (industry interests) wishing to participate in the selection of an 
    appropriate member of a particular panel may nominate one or more 
    qualified persons to represent industry interests. Persons who nominate 
    themselves as industry representatives for the panels will not 
    participate in the selection process. It is, therefore, recommended 
    that all nominations be made by someone with an organization, trade 
    association, or firm who is willing to participate in the selection 
    process.
        Nominees shall be full-time employees of firms that manufacture 
    products that would come before the panel, or consulting firms that 
    represent manufacturers. Nominations shall include a complete 
    curriculum vitae of each nominee. The term of office is up to 4 years, 
    depending on the appointment date.
    
    Selection Procedures
    
    Consumer Representatives
    
        Selection of members representing consumer interests is conducted 
    through procedures which include use of a consortium of consumer 
    organizations which has the responsibility for recommending candidates 
    for the agency's selection. Candidates should possess appropriate 
    qualifications to understand and contribute to the committee's work.
    
    Industry Representatives
    
        Regarding nominations for members representing the interests of 
    industry, a letter will be sent to each person that has made a 
    nomination, and to those organizations indicating an interest in 
    participating in the selection process, together with a complete list 
    of all such organizations and the nominees. This letter will state that 
    it is the responsibility of each nominator or organization indicating 
    an interest in
    
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    participating in the selection process to consult with the others in 
    selecting a single member representing industry interests for the panel 
    within 60 days after receipt of the letter. If no individual is 
    selected within 60 days, the agency will select the nonvoting member 
    representing industry interests.
        This notice is issued under the Federal Advisory Committee Act (5 
    U.S.C. app. 2) and 21 CFR part 14, relating to advisory committees.
        Dated: June 26, 1998.
    Michael A. Friedman,
    Deputy Commissioner for Operations.
    [FR Doc. 98-17601 Filed 7-1-98; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
07/02/1998
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice.
Document Number:
98-17601
Dates:
Nominations should be received by (insert date 30 days after date of publication in the Federal Register), for vacancies listed in this notice.
Pages:
36242-36244 (3 pages)
PDF File:
98-17601.pdf