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Record 1 of 9
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Title
Guidance for clinical investigators, sponsors, and IRBs [electronic resource] : adverse event reporting to IRBs : improving human subject protection.
Imprint
Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of the Commissioner, [2009]
Connect to
Connect to https://permanent.fdlp.gov/lps115951/UCM126572.pdf
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Location
Call No.
OPAC Message
Status
Axe Federal Documents Online
HE 20.4002:AD 9/4
---
Available
Description
1 online resource (6 p.).
Note
"Procedural".
"January 2009".
Subject
Clinical trials -- Reporting.
Human experimentation in medicine.
Institutional review boards (Medicine) -- Government policy -- United States.
Added Author
United States. Food and Drug Administration. Office of the Commissioner.
Added Title
Adverse event reporting to IRBs
Improving human subject protection
Gpo Item No.
0475 (online)
Sudoc No.
HE 20.4002:AD 9/4
Available items only
