Emergency use authorization of medical products and related authorities: guidance for industry and other stakeholders

Emergency use authorization of medical products and related authorities: guidance for industry and other stakeholders

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. Office of the Commissioner, issuing body.
United States. Food and Drug Administration. Office of the Chief Scientist. Office of Counterterrorism and Emerging Threats, issuing body.
Publication:
Silver Spring, MD : Food and Drug Administration, U.S. Department of Health and Human Services, January 2017
Language(s):
English
Format:
Text
Subject(s):
Civil Defense -- legislation & jurisprudence
Device Approval
Drug Approval
Emergencies
Terrorism
United States
United States. Department of Health and Human Services
United States. Department of Homeland Security
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 (iv, 45 pages)).
NLM Unique ID:
101712946 (See catalog record)
Permanent Link:
http://resource.nlm.nih.gov/101712946