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Guidance for industry : IRB review of stand-alone HIPAA authorizations under FDA regulations.

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Format:
Book
Government document
Contributor:
United States. Food and Drug Administration. Office of the Commissioner
Language:
English
Subjects (All):
Institutional review boards (Medicine)--Government policy--United States.
Institutional review boards (Medicine).
United States.
Physical Description:
1 online resource (10 pages)
Other Title:
IRB review of stand-alone HIPAA authorizations under FDA regulations
Place of Publication:
Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of the Commissioner, [2003]
Notes:
"Final guidance."
"October 21, 2003."
OCLC:
432329182

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