Evaluation of devices used with regenerative medicine advanced therapies

Evaluation of devices used with regenerative medicine advanced therapies

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.
United States. Food and Drug Administration. Office of the Commissioner. Office of Special Medical Programs. Office of Combination Products, issuing body.
Center for Biologics Evaluation and Research (U.S.), issuing body.
Center for Devices and Radiological Health (U.S.), issuing body.
Publication:
Silver Spring, MD : Center for Biologics Evaluation and Research, February 2019
Language(s):
English
Format:
Text
Subject(s):
Device Approval
Equipment and Supplies -- classification
Regenerative Medicine -- classification
Regenerative Medicine -- instrumentation
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, 11 pages)).
NLM Unique ID:
101760001 (See catalog record)
Permanent Link:
http://resource.nlm.nih.gov/101760001