NATIONAL WORKSHOPS ON THE PROTECTION OF HUMAN SUBJECTS NIH GUIDE, Volume 21, Number 5, February 7, 1992 P.T. 42 Keywords: Human Subjects Policy National Institutes of Health Food and Drug Administration The National Institutes of Health (NIH) and the Food and Drug Administration (FDA) are sponsoring a series of workshops on the 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: SOUTH MIDWESTERN WORKSHOP DATES: February 20 and 21, 1992 WORKSHOP SITE: San Antonio, TX SPONSORS: University of Texas Health Science Center at San Antonio 7703 Floyd Curl Drive San Antonio, TX 78284-7972 St. Mary's University One Camino Santa Maria San Antonio, TX 78228-8572 REGISTRATION CONTACT: Ms. Angie Khan Institutional Coordinator of Research Review University of Texas Health Science Center at San Antonio 7703 Floyd Curl Drive (Room 402L) San Antonio, TX 78284-7972 Telephone: (512) 567-2351 TOPIC: Identifying and Assessing Risks in Human Subject Research For further information regarding these workshops and future NIH/FDA National Protection of Human Subjects Workshops, please contact: Ms. Darlene Marie Ross Executive Assistant for Education Division of Human Subject Protections Office for Protection from Research Risks National Institutes of Health 9000 Rockville Pike Building 31, Room 5B59 Bethesda, MD 20892 Telephone: (301) 496-8101 .
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Office of Extramural Research (OER) |
National Institutes of Health (NIH) 9000 Rockville Pike Bethesda, Maryland 20892 |
Department of Health and Human Services (HHS) |
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