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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-2009-N-0487-0003
Document Type: Notice
Agency: Food And Drug Administration
Topics: No Topics associated with this document
Federal Register Number: 2010-10782
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Details Information

Abstract: Approval Expires on February 28, 2013
Document Subtype: NAL-Notice of Approval
Received Date: May 07 2010, at 10:26 AM Eastern Daylight Time
Start-End Page: 25268 - 25268
Page Count: 1

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