eLaws | eCases | United States Code | Federal Courts |
Home » Rulemaking » Draft Guidance for Industry and Staff; Availability: In Vitro Companion Diagnostic Devices

Draft Guidance for Industry and Staff; Availability: In Vitro Companion Diagnostic Devices

Document ID: FDA-2011-D-0215-0003
Document Type: Notice
Agency: Food And Drug Administration
Topics: No Topics associated with this document
Federal Register Number: 2011-21226
View Document:  View as format pdf View as format html

Details Information

Document Subtype: Notice of Extension
Received Date: August 19 2011, at 12:00 AM Eastern Daylight Time
Start-End Page: 51993 - 51993
Page Count: 1
Comment Start Date: August 19 2011, at 12:00 AM Eastern Standard Time
Comment Due Date: October 12 2011, at 11:59 PM Eastern Standard Time

Comments

    View All
Total: 26
American National Red Cross - Comment
Posted: 09/22/2011     ID: FDA-2011-D-0215-0007

Oct 12,2011 11:59 PM ET
RCQ Consulting - Comment
Posted: 09/22/2011     ID: FDA-2011-D-0215-0009

Oct 12,2011 11:59 PM ET
Amgen, Inc - Comment
Posted: 09/23/2011     ID: FDA-2011-D-0215-0011

Oct 12,2011 11:59 PM ET
kevin arnold - Comment
Posted: 10/13/2011     ID: FDA-2011-D-0215-0012

Oct 12,2011 11:59 PM ET
Pharmaceutical Research and Manufacturers of America (PhRMA) - Comment
Posted: 10/13/2011     ID: FDA-2011-D-0215-0013

Oct 12,2011 11:59 PM ET

Related Documents

Total: 0
No documents available.