eLaws
|
eCases
|
United States Code
|
Federal Courts
|
Sign In
Sign Up
eLaws
eCases »
United States Code
Federal Courts »
Home
»
Rulemaking
» Draft Guidance for Industry onClinical Pharmacogenomics; Availability: Premarketing Evaluation in Early Phase Clinical Studies
Draft Guidance for Industry onClinical Pharmacogenomics; Availability: Premarketing Evaluation in Early Phase Clinical Studies
Document ID:
FDA-2011-D-0082-0001
Document Type:
Notice
Agency:
Food And Drug Administration
Topics:
No Topics associated with this document
Federal Register Number:
2011-3679
View Document:
Details Information
Document Subtype:
NAD-Notice of Availability of Data
Received Date:
February 18 2011, at 12:00 AM Eastern Standard Time
Start-End Page:
9583 - 9584
Page Count:
2
Comment Start Date:
February 18 2011, at 12:00 AM Eastern Standard Time
Comment Due Date:
April 19 2011, at 11:59 PM Eastern Standard Time
Comments
View All
Total:
14
PhRMA - Comment
Posted:
04/26/2011
ID:
FDA-2011-D-0082-0008
Comment Period Closed
Apr 19,2011 11:59 PM ET
Novo Nordisk Inc. - Comment
Posted:
04/06/2011
ID:
FDA-2011-D-0082-0004
Comment Period Closed
Apr 19,2011 11:59 PM ET
Boehringer Ingelheim Pharmaceutical, Inc - Comment
Posted:
04/14/2011
ID:
FDA-2011-D-0082-0005
Comment Period Closed
Apr 19,2011 11:59 PM ET
American Medical Association (AMA) - Comment
Posted:
04/14/2011
ID:
FDA-2011-D-0082-0006
Comment Period Closed
Apr 19,2011 11:59 PM ET
Novartis Pharmaceuticals Corp. - Comment
Posted:
04/14/2011
ID:
FDA-2011-D-0082-0007
Comment Period Closed
Apr 19,2011 11:59 PM ET
Related Documents
Total:
0
No documents available.
Draft Guidance for Industry onClinical Pharmacogenomics; Availability: Premarketing Evaluation in Early Phase Clinical Studies
Details Information
Comments
View AllPosted: 04/26/2011 ID: FDA-2011-D-0082-0008
Apr 19,2011 11:59 PM ET
Posted: 04/06/2011 ID: FDA-2011-D-0082-0004
Apr 19,2011 11:59 PM ET
Posted: 04/14/2011 ID: FDA-2011-D-0082-0005
Apr 19,2011 11:59 PM ET
Posted: 04/14/2011 ID: FDA-2011-D-0082-0006
Apr 19,2011 11:59 PM ET
Posted: 04/14/2011 ID: FDA-2011-D-0082-0007
Apr 19,2011 11:59 PM ET
Related Documents