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Guidance for clinical investigators, sponsors, and IRBs : adverse event reporting to IRBs : improving human subject protection.
- Format:
- Book
- Government document
- Language:
- English
- Subjects (All):
- Clinical trials--Reporting.
- Clinical trials.
- Human experimentation in medicine.
- Institutional review boards (Medicine)--Government policy--United States.
- Institutional review boards (Medicine).
- United States.
- Physical Description:
- 1 online resource (6 pages)
- Other Title:
- Adverse event reporting to IRBs
- Improving human subject protection
- Place of Publication:
- Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of the Commissioner, [2009]
- Notes:
- "Procedural."
- "January 2009."
- OCLC:
- 430536912
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