Guidance for industry : sterile drug products produced by aseptic processing, current good manufacturing practice.

Bibliographic Details
Corporate Authors:	Center for Drug Evaluation and Research (U.S.), Center for Biologics Evaluation and Research (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:	Drugs > Sterilization > United States. Asepsis and antisepsis.
Online Access:	https://purl.fdlp.gov/GPO/LPS116640

Description
Item Description:	"Center for Biologics Evaluation and Research (CBER)." "Office of Regulatory Affairs (ORA)." "Pharmaceutical CGMPs." "September 2004." Electronic resource.
Physical Description:	1 online resource (59 pages)
Bibliography:	Includes bibliographical references (pages 54-55).