eLaws
|
eCases
|
United States Code
|
Federal Courts
|
Sign In
Sign Up
eLaws
eCases »
United States Code
Federal Courts »
Home
»
Rulemaking
» Generic Drug User Fee Amendments of 2012; Regulatory Science Initiatives Public Hearing; Request for Comments
Generic Drug User Fee Amendments of 2012; Regulatory Science Initiatives Public Hearing; Request for Comments
Document ID:
FDA-2013-N-0402-0001
Document Type:
Proposed Rule
Agency:
Food And Drug Administration
Topics:
No Topics associated with this document
Federal Register Number:
2013-11007
CFR Citation:
21 CFR Part 15
View Document:
Details Information
Document Subtype:
Public Meeting
Received Date:
May 09 2013, at 12:00 AM Eastern Daylight Time
Start-End Page:
27113 - 27115
Page Count:
3
Comment Start Date:
May 9 2013, at 12:00 AM Eastern Standard Time
Comment Due Date:
June 7 2013, at 11:59 PM Eastern Standard Time
Comments
Total:
4
Peter Rawson Byron - Comment
Posted:
06/04/2013
ID:
FDA-2013-N-0402-0002
Comment Period Closed
Jun 07,2013 11:59 PM ET
The People's Pharmacy - Comment
Posted:
06/20/2013
ID:
FDA-2013-N-0402-0003
Comment Period Closed
Jun 07,2013 11:59 PM ET
Waters Technologies Corporation - Comment
Posted:
06/20/2013
ID:
FDA-2013-N-0402-0004
Comment Period Closed
Jun 07,2013 11:59 PM ET
Richard H Guy - Comment
Posted:
06/20/2013
ID:
FDA-2013-N-0402-0005
Comment Period Closed
Jun 07,2013 11:59 PM ET
Related Documents
Total:
2
Food and Drug Administration Actions Related to Nicotine Replacement Therapies and Smoking-Cessation Products; Report to Congress on Innovative Products and Treatments for Tobacco Dependence; Public Hearing; Extension of Comment Period
Actions Related to Nicotine Replacement Therapies and Smoking-Cessation Products: Report to Congress on Innovative Products and Treatments for Tobacco Dependence; Public Hearing
Generic Drug User Fee Amendments of 2012; Regulatory Science Initiatives Public Hearing; Request for Comments
Details Information
Comments
Posted: 06/04/2013 ID: FDA-2013-N-0402-0002
Jun 07,2013 11:59 PM ET
Posted: 06/20/2013 ID: FDA-2013-N-0402-0003
Jun 07,2013 11:59 PM ET
Posted: 06/20/2013 ID: FDA-2013-N-0402-0004
Jun 07,2013 11:59 PM ET
Posted: 06/20/2013 ID: FDA-2013-N-0402-0005
Jun 07,2013 11:59 PM ET
Related Documents