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Draft Guidance for Industry: Use of Nucleic Acid Tests on Pooled and Individual Samples from Donors of Whole Blood and Blood Components, etc.

Document ID: FDA-2011-D-0799-0001
Document Type: Notice
Agency: Food And Drug Administration
Topics: No Topics associated with this document
Federal Register Number: 2011-30449
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Details Information

Document Subtype: Notice of Availability
Received Date: November 28 2011, at 12:00 AM Eastern Standard Time
Start-End Page: 72950 - 72951
Page Count: 2
Comment Start Date: November 28 2011, at 12:00 AM Eastern Standard Time
Comment Due Date: January 27 2012, at 11:59 PM Eastern Standard Time

Comments

    View All
Total: 6
Plasma Protein Therapeutics Association (PPTA) - Comment
Posted: 02/13/2012     ID: FDA-2011-D-0799-0003

Jan 27,2012 11:59 PM ET
Roche Molecular Systems, Inc. - Comment
Posted: 02/13/2012     ID: FDA-2011-D-0799-0004

Jan 27,2012 11:59 PM ET
America's Blood Centers - Comment
Posted: 02/13/2012     ID: FDA-2011-D-0799-0005

Jan 27,2012 11:59 PM ET
Roche Molecular Systems, Inc. (RMS) - Comment
Posted: 04/17/2012     ID: FDA-2011-D-0799-0006

Jan 27,2012 11:59 PM ET
Viacord Processing Laboratory (VPL) - Comment
Posted: 04/17/2012     ID: FDA-2011-D-0799-0007

Jan 27,2012 11:59 PM ET

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