M4 organization of the Common Technical Document for the Registration of Pharmaceuticals for Human Use

M4 organization of the Common Technical Document for the Registration of Pharmaceuticals for Human Use

Collection:
Health Policy and Services Research
Series Title(s):
Guidance for industry
Contributor(s):
United States. Department of Health and Human Services, issuing body.
United States. Food and Drug Administration, issuing body.
Center for Biologics Evaluation and Research (U.S.), issuing body.
Center for Drug Evaluation and Research (U.S.), issuing body.
Publication:
Silver Spring, MD : Center for Drug Evaluation and Research, October 2017
Language(s):
English
Format:
Text
Subject(s):
Documentation -- standards
Drug Approval
Canada
Europe
Japan
Switzerland
United States
United States. Department of Health and Human Services
United States. Food and Drug Administration
Genre(s):
Guideline
Technical Report
Copyright:
The National Library of Medicine believes this item to be in the public domain. (More information)
Extent:
1 online resource (1 PDF file (27 pages))
Illustrations:
Illustrations
NLM Unique ID:
101719844 (See catalog record)
Permanent Link:
http://resource.nlm.nih.gov/101719844