eLaws
|
eCases
|
United States Code
|
Federal Courts
|
Sign In
Sign Up
eLaws
eCases »
United States Code
Federal Courts »
Home
»
Rulemaking
» Draft Guidance for Industry; Availability: Chronic Hepatitis C Virus Infection; Developing Direct-Acting Antiviral Agents forTreatment
Draft Guidance for Industry; Availability: Chronic Hepatitis C Virus Infection; Developing Direct-Acting Antiviral Agents forTreatment
Document ID:
FDA-2010-D-0462-0001
Document Type:
Notice
Agency:
Food And Drug Administration
Topics:
No Topics associated with this document
Federal Register Number:
2010-22806
View Document:
Details Information
Document Subtype:
NAD-Notice of Availability of Data
Received Date:
September 13 2010, at 12:00 AM Eastern Daylight Time
Start-End Page:
55797 - 55798
Page Count:
2
Comment Start Date:
September 14 2010, at 12:00 AM Eastern Standard Time
Comment Due Date:
November 15 2010, at 11:59 PM Eastern Standard Time
Comments
View All
Total:
12
Merck & Co, Inc. - Comment
Posted:
11/18/2010
ID:
FDA-2010-D-0462-0004
Comment Period Closed
Nov 15,2010 11:59 PM ET
Novartis - Comment
Posted:
11/18/2010
ID:
FDA-2010-D-0462-0006
Comment Period Closed
Nov 15,2010 11:59 PM ET
GlaxoSmithKline - Comment
Posted:
11/18/2010
ID:
FDA-2010-D-0462-0007
Comment Period Closed
Nov 15,2010 11:59 PM ET
Merck & Company - Comment
Posted:
11/18/2010
ID:
FDA-2010-D-0462-0008
Comment Period Closed
Nov 15,2010 11:59 PM ET
Gilead Sciences Inc. - Comment
Posted:
11/18/2010
ID:
FDA-2010-D-0462-0010
Comment Period Closed
Nov 15,2010 11:59 PM ET
Related Documents
Total:
0
No documents available.
Draft Guidance for Industry; Availability: Chronic Hepatitis C Virus Infection; Developing Direct-Acting Antiviral Agents forTreatment
Details Information
Comments
View AllPosted: 11/18/2010 ID: FDA-2010-D-0462-0004
Nov 15,2010 11:59 PM ET
Posted: 11/18/2010 ID: FDA-2010-D-0462-0006
Nov 15,2010 11:59 PM ET
Posted: 11/18/2010 ID: FDA-2010-D-0462-0007
Nov 15,2010 11:59 PM ET
Posted: 11/18/2010 ID: FDA-2010-D-0462-0008
Nov 15,2010 11:59 PM ET
Posted: 11/18/2010 ID: FDA-2010-D-0462-0010
Nov 15,2010 11:59 PM ET
Related Documents