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Agency Information Collection Activities; Proposals, Submissions, and Approvals: Adverse Experience Reporting for Licensed Biological Products; and General Records

Document ID: FDA-2011-N-0231-0003
Document Type: Notice
Agency: Food And Drug Administration
Topics: No Topics associated with this document
Federal Register Number: 2011-17675
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Details Information

Document Subtype: General Notice
Received Date: July 14 2011, at 12:00 AM Eastern Daylight Time
Start-End Page: 41504 - 41506
Page Count: 3
Comment Start Date: July 14 2011, at 12:00 AM Eastern Standard Time
Comment Due Date: August 15 2011, at 11:59 PM Eastern Standard Time

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