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Research Unique Device Identification Medical device Center for Devices and Radiological Health Adverse Event Reporting System Clinical research Electronic health record Adverse event Premarket approval Food and Drug Administration Medicine Health		Add to Reading List Source URL: www.fda.gov Download Document from Source Website File Size: 403,12 KB Share Document on Facebook

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	Federal Register / Vol. 80, NoWednesday, May 6, Notices Submit electronic comments on the draft guidance to http:// www.regulations.gov. Submit written comments to the Division of Dockets Management (HFA– DocID: 1aGhA - View Document
	This document is scheduled to be published in the Federal Register onand available online at http://federalregister.gov/a, and on FDsys.govP DEPARTMENT OF HEALTH AND HUMAN SERVICES DocID: 1akUI - View Document
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