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FDA clinical investigator information sheets [microform].

Published
Rockville, MD : Dept. of Health & Human Services, Public Health Service, Food and Drug Administration, [1991]
Physical Description
54 pages
Additional Creators
United States. Food and Drug Administration

Availability

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Contents
Required recordkeeping in clinical investigations -- Informed consent and the clinical investigator -- FDA inspections of clinical investigators -- Clinical investigator regulatory sanctions -- Treatment use of investigational drugs -- Placebo-controlled and active controlled drug study designs.
Report Numbers
HE 20.4002:C 61
Subject(s)
Note
Caption title.
"May 1989."
Bibliography Note
Includes bibliographical references (page 47).
Reproduction Note
Microfiche. Washington, D.C. : U.S. G.P.O., 1992. 1 microfiche : negative ; 11 x 15 cm.
View MARC record | catkey: 1487337