WORKSHOP ON HUMAN SUBJECT PROTECTIONS Release Date: June 25, 1998 P.T. National Institutes of Health Food and Drug Administration The National Institutes of Health (NIH) and the Food and Drug Administration (FDA) are continuing to sponsor a series of workshops on responsibilities of researchers, Institutional Review Boards (IRBs), and institutional officials for the protection of human subjects in research. The workshops are open to everyone with an interest in research involving human subjects. The meetings should be of special interest to those persons currently serving or about to begin serving as a member of an IRB. Issues discussed at these workshops are relevant to all other Public Health Service agencies. The current schedule includes the following: DATES: August 6-7, 1998 TITLE: Pressure Points in Human Subjects Research LOCATION: University of Rochester, Rochester, NY SPONSORS: University of Rochester, Rochester, NY REGISTRATION CONTACT: Mr. Clint Lewis Conference and Events Office University of Rochester RC Box 270041 Rochester, NY 14627-0041 Telephone: (716) 275-4111 Email: clewis@admin.rochester.edu REGISTRATION FEE: $200 DESCRIPTION: This program is intended for Institutional Review Board (IRB) chairs, members, administrators, researchers, and members of the community. Topics include updates on latest federal policies and initiatives such as the new inclusion of children guidance, information about review/conduct of clinical trials, consent/assent issues in special populations, and innovations for IRBs. INQUIRIES For further information regarding these workshops or future NIH/FDA National Human Subject Protections Workshops, contact: Ms. Darlene Marie Ross Office for Protection from Research Risks National Institutes of Health 6100 Executive Boulevard, Suite 3B01 Rockville, MD 20892-7507 Telephone: (301) 435-5648 FAX: (301) 402-0527 Email: dr20a@nih.gov
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