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» Current Good Manufacturing Practice Requirements for Combination Products; Extension of Comment Period
Current Good Manufacturing Practice Requirements for Combination Products; Extension of Comment Period
Document ID:
FDA-2009-N-0435-0004
Document Type:
Proposed Rule
Agency:
Food And Drug Administration
Topics:
No Topics associated with this document
Federal Register Number:
E9-26966
CFR Citation:
21 CFR 4
View Document:
Details Information
Document Subtype:
NEC-Notice of Extension
Received Date:
November 09 2009, at 12:35 PM Eastern Standard Time
Start-End Page:
57973 - 57974
Page Count:
2
Comment Start Date:
November 10 2009, at 12:00 AM Eastern Standard Time
Comment Due Date:
February 5 2010, at 11:59 PM Eastern Standard Time
Comments
View All
Total:
17
Novo Nordisk, Inc. - Comment
Posted:
01/26/2010
ID:
FDA-2009-N-0435-0009
Comment Period Closed
Feb 05,2010 11:59 PM ET
American Medical Systems (AMS) - Comment
Posted:
01/26/2010
ID:
FDA-2009-N-0435-0010
Comment Period Closed
Feb 05,2010 11:59 PM ET
Michael Barbush - Comment
Posted:
02/01/2010
ID:
FDA-2009-N-0435-0012
Comment Period Closed
Feb 05,2010 11:59 PM ET
Rocky Mountain Regulatory Affairs Society - Comment
Posted:
02/04/2010
ID:
FDA-2009-N-0435-0015
Comment Period Closed
Feb 05,2010 11:59 PM ET
Robert L. Dana - Comment
Posted:
02/04/2010
ID:
FDA-2009-N-0435-0016
Comment Period Closed
Feb 05,2010 11:59 PM ET
Related Documents
Total:
3
Postmarketing Safety Reporting for Combination Products; Extension of Comment Period
Current Good Manufacturing Practice Requirements for Combination Products; Correction
Current Good Manufacturing Practice Requirements for Combination Products
Current Good Manufacturing Practice Requirements for Combination Products; Extension of Comment Period
Details Information
Comments
View AllPosted: 01/26/2010 ID: FDA-2009-N-0435-0009
Feb 05,2010 11:59 PM ET
Posted: 01/26/2010 ID: FDA-2009-N-0435-0010
Feb 05,2010 11:59 PM ET
Posted: 02/01/2010 ID: FDA-2009-N-0435-0012
Feb 05,2010 11:59 PM ET
Posted: 02/04/2010 ID: FDA-2009-N-0435-0015
Feb 05,2010 11:59 PM ET
Posted: 02/04/2010 ID: FDA-2009-N-0435-0016
Feb 05,2010 11:59 PM ET
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