Guidance for clinical investigators, sponsors, and IRBs : adverse event reporting to IRBs : improving human subject protection.

Bibliographic Details
Corporate Author:	United States. Food and Drug Administration. Office of the Commissioner
Format:	Government Document eBook
Language:	English
Published:	Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of the Commissioner, [2009]
Subjects:	Clinical trials > Reporting. Human experimentation in medicine. Institutional review boards (Medicine) > Government policy > United States.
Online Access:	https://purl.fdlp.gov/GPO/LPS115951

Available Online