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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