eLaws
|
eCases
|
United States Code
|
Federal Courts
|
Sign In
Sign Up
eLaws
eCases »
United States Code
Federal Courts »
Home
»
Rulemaking
» Modernizing the Regulation of Clinical Trials and Approaches to Good Clinical Practice; Public Hearing; Request for Comments
Modernizing the Regulation of Clinical Trials and Approaches to Good Clinical Practice; Public Hearing; Request for Comments
Document ID:
FDA-2012-N-0170-0001
Document Type:
Notice
Agency:
Food And Drug Administration
Topics:
No Topics associated with this document
Federal Register Number:
2012-05476
CFR Citation:
21 CFR Chapter I
View Document:
Details Information
Abstract:
Public Hearing on 4/23-24/2012 Registration due 4/2/2012 Comments due 5/31/2012
Document Subtype:
Notice of Hearing
Received Date:
March 06 2012, at 12:00 AM Eastern Standard Time
Start-End Page:
13513 - 13516
Page Count:
4
Comment Start Date:
March 7 2012, at 12:00 AM Eastern Standard Time
Comment Due Date:
May 31 2012, at 11:59 PM Eastern Standard Time
Comments
View All
Total:
30
PSPC Alliance - Comment
Posted:
04/16/2012
ID:
FDA-2012-N-0170-0002
Comment Period Closed
May 31,2012 11:59 PM ET
John Anthony Laczin - Comment
Posted:
04/16/2012
ID:
FDA-2012-N-0170-0003
Comment Period Closed
May 31,2012 11:59 PM ET
Association of Clinical Research Organizations (ACRO) - Comment
Posted:
04/16/2012
ID:
FDA-2012-N-0170-0004
Comment Period Closed
May 31,2012 11:59 PM ET
Regulatory Education and Action for Patients (REAP) - Comment
Posted:
04/16/2012
ID:
FDA-2012-N-0170-0005
Comment Period Closed
May 31,2012 11:59 PM ET
National Patient Advocate Foundation (NPAF) - Comment
Posted:
04/16/2012
ID:
FDA-2012-N-0170-0006
Comment Period Closed
May 31,2012 11:59 PM ET
Related Documents
More
Total:
15
Food and Drug Administration Safety and Innovation Act Title VII--Drug Supply Chain; Standards for Admission of Imported Drugs, Registration of Commercial Importers and Good Importer Practices; Notification of Public Meeting; Request for Comments
Food and Drug Administration Safety and Innovation Act Title VII--Drug Supply Chain; Standards for Admission of Imported Drugs, Registration of Commercial Importers and Good Importer Practices; Notification of Public Meeting; Request for Comments
Food and Drug Administration Safety and Innovation Act Title VII--Drug Supply Chain; Standards for Admission of Imported Drugs, Registration of Commercial Importers and Good Importer Practices; Notification of Public Meeting; Request for Comments
Administrative Detention under the Food and Drug Administration Safety and Innovation Act
Tobacco Product Manufacturing Practice; Establishment of a Public Docket
Regulatory New Drug Review: Solutions for Study Data Exchange Standards; Meeting; Request for Comments; Correction
Regulatory New Drug Review: Solutions for Study Data Exchange Standards; Meeting; Request for Comments
See FDA-2012-N-0780-0001
Revision of Organization and Conforming Changes to Regulations
Preemption Review
Revised Guidance on Marketed Unapproved Drugs; Availability: Marketed New Drugs Without Approved NDAs or ANDAs
Periodic Reviews of Existing Regulations
Food Safety Modernization Act, Focus on Preventive Controls for Facilities; Notice of Public Meeting
Revision of Organization and Conforming Changes to Regulations
Withdrawal of Certain Proposed Rules and Other Proposed Actions
Modernizing the Regulation of Clinical Trials and Approaches to Good Clinical Practice; Public Hearing; Request for Comments
Details Information
Comments
View AllPosted: 04/16/2012 ID: FDA-2012-N-0170-0002
May 31,2012 11:59 PM ET
Posted: 04/16/2012 ID: FDA-2012-N-0170-0003
May 31,2012 11:59 PM ET
Posted: 04/16/2012 ID: FDA-2012-N-0170-0004
May 31,2012 11:59 PM ET
Posted: 04/16/2012 ID: FDA-2012-N-0170-0005
May 31,2012 11:59 PM ET
Posted: 04/16/2012 ID: FDA-2012-N-0170-0006
May 31,2012 11:59 PM ET
Related Documents
More