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Update on FDA regulation of in vitro diagnostic devices

S Gutman1, K Richter, S Alpert

  • 1Office of Device Evaluation, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, MD 20850, USA. sig@cdrh.fda.gov

JAMA
|July 21, 1998
PubMed
Abstract

No abstract available in PubMed .

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