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 Date: 2009-06-10 21:38:09Pharmaceutical sciences Center for Devices and Radiological Health Medical device Premarket approval Regulatory requirement Adverse event Criticism of the Food and Drug Administration Title 21 CFR Part 11 Food and Drug Administration Medicine Health |
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foSU.V1l:$ofJ (-~:1 -l MEMORANDUM | Microsoft PowerPoint - dittoDocID: 1gc7K - View Document |
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| Federal Register / Vol. 80, NoWednesday, May 6, Notices Submit electronic comments on the draft guidance to http:// www.regulations.gov.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 SERVICESDocID: 1akUI - View Document |
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