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Guidance for industry : PAT, a framework for innovative pharmaceutical development, manufacturing, and quality assurance.

Bibliographic Details
Corporate Authors: Center for Drug Evaluation and Research (U.S.), Center for Veterinary Medicine (U.S.), 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, [2004]
Subjects:
Drug development > Government policy > United States.
Drug factories > Government policy > United States.
Quality assurance > Government policy > United States.
Online Access:https://purl.fdlp.gov/GPO/LPS116481
Description
Item Description:"Center for Veterinary Medicine (CVM)."
"Office of Regulatory Affairs (ORA)."
"Pharmaceutical CGMPs."
"September 2004."
Electronic resource.
Physical Description:1 online resource (16 pages)
Bibliography:Includes bibliographical references (page 16).