95-1381. Notice of a Regional Public Hearing of the Commission on Research Integrity  

  • [Federal Register Volume 60, Number 13 (Friday, January 20, 1995)]
    [Notices]
    [Page 4168]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 95-1381]
    
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Notice of a Regional Public Hearing of the Commission on Research 
    Integrity
    
        Pursuant to Pub. L. 92-463, notice is hereby given of a public 
    hearing and meeting, respectively, of the Commission on Research 
    Integrity on Thursday and Friday, February 9 and 10, 1995, from 9:00 
    a.m. to 5 p.m. at University of California-San Francisco in the 
    auditorium of the Laurel Heights Conference Center at 3333 California 
    Street, San Francisco, CA 94118. The sessions will be open to the 
    public. Interested parties are advised to call the Executive Secretary 
    shortly before the meeting to verify the date, place, and agenda.
        The mandate of the Commission is to develop recommendations for the 
    Secretary of the Department of Health and Human Services (DHHS) and the 
    Congress on the administration of Section 493 of the Public Health 
    Service Act, as amended by and added to, by Section 161 of the NIH 
    Revitalization Act of 1993.
        It has become increasingly clear to the Commission that the current 
    DHHS and institutional oversight of research integrity deserves serious 
    attention. Also, the Commission has confirmed that there are no quick 
    and easy answers as it searches for fair, effective, and realistic 
    administrative solutions to these issues. Therefore, an essential 
    component of the Commission's information-gathering is to interact 
    extensively with all relevant constituencies of the scientific 
    community--including junior and senior scientists, witnesses, 
    respondents, and academic administrators--to understand their 
    particular experiences and perspectives and to explore possible 
    improvements.
        Three major areas are currently of great interest to the 
    Commission:
        1. A New Definition of Research Misconduct. The Commission believes 
    that any definition needs to address the full extent of serious 
    research misconduct, but must avoid a definition that is too broad, 
    vague, and potentially unfair. In addition, a two-tiered approach for 
    research integrity, and failures thereof, would be useful; it would 
    emphasize institutional responsibility, and reserve an oversight role 
    for the Federal Government.
        2. Assurance for Institutions and Accountability for Federally-
    Funded Research. The Commission is considering that each institution 
    receiving Federal funds develop and submit for Federal review and 
    approval assurances concerning the establishment and implementation of: 
    (a) good research practices and professional norms; (b) procedures for 
    disseminating that information throughout its community; and (c) 
    educational activities designed to foster practice of the highest 
    ethical standards in the conduct of research with particular emphasis 
    on beginning researchers. Topics affecting good research practices that 
    might be addressed in institutional assurances include: data recording 
    and retention; supervisory responsibility; authorship practices; 
    protection of witnesses; and other professional conduct bearing 
    directly on the integrity of Federally-supported research.
        3. Bill of Rights for Witnesses. Testimony from witnesses (also 
    called ``whistleblowers'') who had challenged perceived research 
    misconduct reaffirms the Commission's mandate to propose effective 
    whistleblower protection rules. Witnesses stated that retaliation 
    occurs with sufficient frequency to have a chilling effect on potential 
    witnesses throughout the research community. The Commission is 
    considering a Witness Bill of Rights and procedures for its 
    implementation.
        The Commission will also continue its discussion of other issues on 
    which the Commission is planning to make recommendations.
        Lengthy statements from witnesses exceeding the 10 or 15 minutes of 
    oral presentation may be submitted in writing to the Executive 
    Secretary before or at the meeting. Each statement will be reviewed by 
    Commission Members.
        Henrietta D. Hyatt-Knorr, Executive Secretary, Commission on 
    Research Integrity, at Rockwall II, Suite 700, 5515 Security Lane, 
    Rockville, MD 20852, (301) 443-5300 or (301) 443-9369 (voice mail), 
    will furnish the meeting agenda, the Committee charter, and a roster of 
    the Committee members upon request. Members of the public wishing to 
    make presentations should contact the Executive Secretary. Depending on 
    the number of presentations and other considerations, the Executive 
    Secretary will allocate a reasonable timeframe for each speaker.
    Henrietta D. Hyatt-Knorr,
    Executive Secretary, Commission on Research Integrity.
    [FR Doc. 95-1381 Filed 1-19-95; 8:45 am]
    BILLING CODE 4160-17-P-M
    
    

Document Information

Published:
01/20/1995
Department:
Health and Human Services Department
Entry Type:
Notice
Document Number:
95-1381
Pages:
4168-4168 (1 pages)
PDF File:
95-1381.pdf