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Agency Information Collection Activities; Proposals, Submissions, and Approvals: Guidance on Informed Consent for In Vitro Diagnostic Device Studies Using Leftover Human Specimens, etc.

Document ID: FDA-2012-N-0560-0003
Document Type: Notice
Agency: Food And Drug Administration
Topics: No Topics associated with this document
Federal Register Number: 2013-11125
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Details Information

Document Subtype: Notice of Approval
Received Date: May 09 2013, at 12:00 AM Eastern Daylight Time
Start-End Page: 27404 - 27404
Page Count: 1
Comment Start Date: May 9 2013, at 12:00 AM Eastern Standard Time

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