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This webpage is a collection of all the guidance documents created by the U.S. Food and Drug Administration's Center for Drug Evaluation and Research. The documents represent what the agency considers good practices. Documents are available on subjects from Compliance and Drug Safety to Current Good Manufacturing Practices and Advertising. The page organizes the documents by subject, allowing one to quickly navigate to the particular subject they are interested in. This site would be useful for anyone studying the pharmaceutical industry as well as for teachers in the discipline. Most documents are available in HTML or PDF, with some being optionally available in Microsoft Word format.
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