NLM Digital Collections

Long term follow-up after administration of human gene therapy products

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.
Publication:
Silver Spring, MD : Center for Biologics Evaluation and Research, January 2020
Language(s):
English
Format:
Text
Subject(s):
Genetic Therapy -- adverse effects
Product Surveillance, Postmarketing
Drug Evaluation, Preclinical
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.
Genre(s):
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 (i, 35 pages))
Illustrations:
Illustrations
NLM Unique ID:
101767662 (See catalog record)
Permanent Link:
http://resource.nlm.nih.gov/101767662