Guidance for industry : Q7A good manufacturing practice guidance for active pharmaceutical ingredients.

Bibliographic Details
Corporate Authors:	Center for Drug Evaluation and Research (U.S.), Center for Biologics Evaluation and Research (U.S.), International Conference on Harmonisation
Format:	Government Document Conference Proceeding eBook
Language:	English
Published:	Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research, [2001]
Subjects:	Drug factories > Quality control. Pharmaceutical chemistry. Drugs > Quality control.
Online Access:	https://purl.fdlp.gov/GPO/LPS113849

Available Online