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Guidance for industry : Prescription Drug Marketing Act (PDMA) requirements, questions and answers.

Bibliographic Details
Corporate Authors: Center for Drug Evaluation and Research (U.S.), United States. Food and Drug Administration. Office of the Commissioner, United States. Food and Drug Administration. Office of Regulatory Affairs
Format: Government Document eBook
Language:English
Published: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Office of the Commissioner : Office of Regulatory Affairs, [2006]
Subjects:
United States. > Prescription Drug Marketing Act of 1987.
United States. > Prescription Drug Amendments of 1992.
Online Access:https://purl.fdlp.gov/GPO/LPS116592

Internet

https://purl.fdlp.gov/GPO/LPS116592

Available Online

Holdings details from Available Online
Call Number: HE 20.4702:P 92/2
 
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HE 20.4702:P 92/2 Available