Form FDA 3674--certifications to accompany drug, biological product, and device applications/submissions: guidance for sponsors, industry, researchers, investigators, and food and drug administration staff
- 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.
United States. Food and Drug Administration. Office of Good Clinical Practice, issuing body.
United States. Food and Drug Administration. Office of Special Medical Programs, issuing body. - Publication:
- Silver Spring, MD : Food and Drug Administration, U.S. Department of Health and Human Services, June 2017
- Language(s):
- English
- Format:
- Text
- Subject(s):
- Device Approval Drug Approval Investigational New Drug Application Access to Information Clinical Trials as Topic Drugs, Investigational Humans 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 (10 pages)).
- NLM Unique ID:
- 101712948 (See catalog record)
- Permanent Link:
- http://resource.nlm.nih.gov/101712948
