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Agency Information Collection Activities; Proposals, Submissions, and Approvals: Draft Guidance for Industry on Postmarketing Adverse Event Reporting for Medical Products, etc.

Document ID: FDA-2008-D-0610-0010
Document Type: Notice
Agency: Food And Drug Administration
Topics: No Topics associated with this document
Federal Register Number: 2011-15799
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Details Information

Document Subtype: General Notice
Received Date: June 24 2011, at 12:00 AM Eastern Daylight Time
Start-End Page: 37124 - 37126
Page Count: 3
Comment Start Date: June 24 2011, at 12:00 AM Eastern Standard Time
Comment Due Date: July 25 2011, at 11:59 PM Eastern Standard Time

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