Guideline for submitting supporting documentation in drug applications for the manufacture of drug substances / Center for Drugs and Biologics, Food and Drug Administration, Department of Health and Human Services.

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Bibliographic Details
Online Access:	Search for the full-text version of this title in HathiTrust
Corporate Author:	Center for Drugs and Biologics (U.S.)
Format:	Government Document Book
Language:	English
Published:	Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, 1987.
Subjects:	Drugs > United States. Legislation, Drug. Drugs > Manufacture > Laws & regulations. Technology, Pharmaceutical > Laws & regulations. Investigational new drug applications. New drug applications. Good manufacturing practices.

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Holdings details from Norlin Library - Government Information - US
Call Number:	HE 20.4208:M 31
HE 20.4208:M 31	Available Place a Hold