Guidance for industry : quality systems approach to pharmaceutical CGMP regulations.

Bibliographic Details
Corporate Authors:	Center for Drug Evaluation and Research (U.S.), Center for Biologics 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, [2006]
Subjects:	Quality of products > United States. Drug development > Government policy > United States. Risk management > United States.
Online Access:	https://purl.fdlp.gov/GPO/LPS116599

Description
Item Description:	"Center for Biologics Evaluation and Research (CBER)." "Center for Veterinary Medicine (CVM)." "Office of Regulatory Affairs (ORA)." "Pharmaceutical CGMPs." "September 2006." Electronic resource.
Physical Description:	1 online resource (28 pages)
Bibliography:	Includes bibliographical references (pages 25-26).