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Office for Human Research Protections (OHRP)

Requests for Public Comment

OHRP invites public comments on the following guidance documents and topics:

  • December 1, 2008 Draft Guidance on Important Considerations for When Participation of Human Subjects in Research is Discontinued

    The Office for Human Research Protections (OHRP), Office of Public Health and Science, is seeking comment on a draft guidance document entitled, “Guidance on Important Considerations for When Participation of Human Subjects in Research is Discontinued.” The draft guidance document, when finalized, would provide OHRP’s first formal guidance on this topic. The draft document is intended primarily for institutional review boards, investigators, and funding agencies that may be responsible for the review or oversight of human subject research conducted or supported by the Department of Health and Human Services. The proposed guidance document would provide guidance on important considerations for when participation of human subjects in research is discontinued, either because a subject voluntarily chooses to discontinue participation during the course of the research, or because an investigator terminates a subject’s participation in the research without regard to the subject’s consent. OHRP will consider comments received before issuing the final guidance document.

    Submit written or electronic comments by January 30, 2009. Comments may be submitted by any of the following methods: (1) E-mail to discontinueparticipation@hhs.gov and include “Guidance on Discontinuation of Subject Participation” in the subject line; (2) Fax: 301-402-2071; (3) Mail/Hand delivery/Courier [For paper, disk, or CD-ROM submissions]: Michael A. Carome, M.D., Captain, U.S. Public Health Service, OHRP, 1101 Wootton Parkway, Suite 200, Rockville, MD 20852.

    Comments received, including any personal information, will be made available to the public upon request.

    The draft guidance can be accessed at:
    http://www.hhs.gov/ohrp/requests/200811guidance.html or
    http://www.hhs.gov/ohrp/requests/200811guidance.pdf.

    A copy of the Federal Register notice announcing the availability of the draft guidance for comment can be accessed at:
    http://edocket.access.gpo.gov/2008/E8-28369.htm or
    http://edocket.access.gpo.gov/2008/pdf/E8-28369.pdf.

    FOR FURTHER INFORMATION CONTACT: Michael A. Carome, M.D., Captain, U.S. Public Health Service, OHRP, 1101 Wootton Parkway, Suite 200, Rockville, MD 20852, 240-453-6900; e-mail Michael.Carome@hhs.gov

Public comments on any OHRP guidance document are welcome at anytime. For any comments not submitted during an identified comment period, please email comments to ohrp@hhs.gov and insert the title of the specific guidance document in the subject field, or submit comments by mail to:

Division of Policy and Assurances
Office for Human Research Protections
1101 Wootton Parkway
Suite 200
Rockville, MD 20852


Prior Requests for Comments


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Last Updated: December 1, 2008

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