Federal Regulation of Human Experimentation, 1975.

Contains CRS monograph by Freeman H. Quimby et al., prepared for the Subcom on Health, compiling history of and current Federal agency policies on management of clinical investigations and welfare of human participants in such investigations.

Bibliographic Details
Corporate Authors:	Library of Congress. Congressional Research Service, ProQuest (Firm)
Format:	Government Document eBook
Language:	English
Published:	[Place of publication not identified] : [publisher not identified], 1975.
Series:	U.S. Congressional Research.
Subjects:	United States. > Department of the Army. United States. > Department of Defense. United States. > Department of Health, Education, and Welfare. Electronic books.
Online Access:	Connect to the full text of this electronic book

Description
Summary:	Contains CRS monograph by Freeman H. Quimby et al., prepared for the Subcom on Health, compiling history of and current Federal agency policies on management of clinical investigations and welfare of human participants in such investigations. Provides list of relevant congressional hearings and texts of public laws (p. 3-11); and discusses evolution of pertinent NIH and FDA guidelines, recent Federal actions, and the National Research Act of 1974 (p. 12-27). Major section of volume (p. 28-236) provides current policies, guidelines, and regulations for the following agencies: HEW, NIH, AEC, FDA, NASA, VA, DOD, Army, AF, and Navy. Concluding section (p. 237-256) summarizes and compares executive and military depts policies, together with concluding editorial comments.
Item Description:	Record is based on bibliographic data in ProQuest U.S. Congressional Research Digital Collection (last viewed June 2010). Reuse except for individual research requires license from ProQuest, LLC. CRS Report. Electronic resource.
Physical Description:	1 online resource.