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:
Online Access:https://purl.fdlp.gov/GPO/LPS121022
Description
Item Description:"Center for Drug Evaluation and Research"--Cover p.
"February 1987."
Electronic resource.
Physical Description:1 electronic resource (17 pages)