Abstract
The Food and Drug Administration (FDA) regularly inspects clinical investigators for a variety of reasons. Characteristics of a clinical study likely to trigger an FDA inspection are described. Items which are routinely examined during an FDA inspection are listed and discussed. Methods are suggested for early identification of clinical investigators who are likely to be inspected, and procedures and techniques are described for the sponsor to assist the clinic in attaining inspection-readiness.
Get full access to this article
View all access options for this article.
References
1.
2.Compliance Program Guidance Manual.
Chapter 48—Bioresearch Monitoring—Human Drugs . Washington, DC ; Food and Drug Administration ; September 1, 1994 .
3.
Bruckheimer
M.
FDA's inspections of clinical investigators . Drug Inf J.
1993 ;27 :213 –216 .
4.
5.Title 21 Code of Federal Regulations . 312.52. Washington, DC : U.S. Government Printing Office ; 1997 .
6.Title 21 Code of Federal Regulations . 312.56. Washington, DC : U.S. Government Printing Office ; 1997 .
7.Title 21 Code of Federal Regulations . 312.66. Washington, DC : U.S. Government Printing Office ; 1997 .
8.Title 21 Code of Federal Regulations . 312.60. Washington, DC : U.S. Government Printing Office ; 1997 .
9.Title 21 Code of Federal Regulations . 312.68. Washington, DC : U.S. Government Printing Office ; 1997 .
10.Investigations Operations Manual. Chapter 5—Establishment Inspection. http://.fda.gov/ora/inspect_ref/iom/96ch5.html, June 1, 1998 .
11.
Spilker
B.
Guide to Clinical Trials.
New York, NY : Raven Press ; 1991 ;450 –452 .
12.
13.Good Clinical Practices in Investigational Product Research Meeting: Notice of meeting.
Federal Register.
1998 ;63 :30001 .
