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 Congresses as Topic European Union International Cooperation Pharmaceutical Preparations -- standards Humans 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