Guideline for submitting documentation for the manufacture of and controls for drug products.

Bibliographic Details
Corporate Authors:	Center for Drugs and Biologics (U.S.), Center for Drug Evaluation and Research (U.S.)
Format:	Government Document eBook
Language:	English
Published:	Rockville, Md. : Center for Drugs and Biologics, Food amd [sic] Drug Administration, U.S. Dept. of Health and Human Services, [1987]
Subjects:	Drugs > Dosage forms > Quality control > Documentation > United States.
Online Access:	https://purl.fdlp.gov/GPO/LPS121022