Medical device postapproval safety monitoring: where does the United States stand?

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Bibliographic Details
Published in:	Circulation Cardiovascular quality and outcomes Vol. 8; no. 1; pp. 124 - 131
Main Authors:	Rajan, Prashant V, Kramer, Daniel B, Kesselheim, Aaron S
Format:	Journal Article
Language:	English
Published:	United States 01-01-2015
Subjects:	Device Approval Humans Patient Safety Product Surveillance, Postmarketing Program Evaluation Registries Risk Assessment Risk Factors United States United States Food and Drug Administration United States equipment and supplies product surveillance, postmarketing registries United States Food and Drug Administration
Online Access:	Get full text
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Description
Bibliography:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
ISSN:	1941-7713 1941-7705
DOI:	10.1161/CIRCOUTCOMES.114.001460