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J Interv Card Electrophysiol ; 47(1): 11-18, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27020440

ABSTRACT

The Food and Drug Administration (FDA) is a large regulatory agency that monitors everything from food, tobacco, and veterinary medicine to pharmaceutical drugs and medical devices. The Mission statement of the CDRH, one of the Centers of the FDA, in its most succinct form is to protect and promote public health. This is accomplished through timely and continued access to safe, effective, and high quality medical devices. This paper aims to review the overarching principles of the Agency's review process for cardiac devices as well as highlight some of the newer programs that FDA has engaged in to facilitate innovation, device development, research, and timely market approval.


Subject(s)
Device Approval/standards , Electrophysiologic Techniques, Cardiac/instrumentation , Electrophysiologic Techniques, Cardiac/standards , Product Surveillance, Postmarketing/standards , Technology Assessment, Biomedical/standards , United States Food and Drug Administration/standards , Device Approval/legislation & jurisprudence , Guidelines as Topic , Technology Assessment, Biomedical/legislation & jurisprudence , United States
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