Achieving Investigator Compliance
Abstract
An important facet of the compliance program is getting the investigator to comply with the various official requirements and regulations in order to increase the data credibility of the trial. The common denominator here is the good clinical practice (GCP) document from the European Community (EC), along with an overview of how the European GCP deals with the compliance problem in general: quality assurance (QA) requirements, of which...
Paper Details
Title
Achieving Investigator Compliance
Published Date
Oct 1, 1993
Journal
Volume
27
Issue
4
Pages
1107 - 1110
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