Home
About the RSC
Frequently Asked Questions
Contact Information
Useful Links
Web Site Update Log
Broadcast Memos
DAIDS RSC Presentations
Regulatory Information
Protocol Development Information
Human Subjects Protection (HSP)
Protocol Registration
Safety and Pharmacovigilance
Case Report Form
(CRF) Management
Clinical Study
Information Office
There are currently no presentations.
Document Title Search
Search Help
RSC Quick Contacts
- Select One -
Regulatory Policy
Informed Consent
Human Subjects Protection
Protocol Registration Policy
EAE and SAE Policy
IND Safety Reports
INSIGHT
Regulatory Documentation
Serious Adverse Events
RSC Safety Information Center
Protocol Registration Office
CSRC/PSRC
Clinical Trials Agreement Support
Human Subjects Protection
Case Report Form Management
Clinical Study Information Office
Package Inserts
Investigator Brochures
Website Change Form
Latest News & Updates
A Pilot Program to Provide Changes in Updated Package Inserts
January 30, 2012
DAIDS Implementation of the New FDA Final Ruling for Mandatory Language Regarding Clinicaltrials.gov for Informed Consents
November 29, 2011
Tips to Be Ready for Expedited Reporting of Adverse Events
November 28, 2011
Adverse Events and DAERS Training at the HVTN Conference
November 7-9, 2011
New Safety and Pharmacovigilance Pages Launched
November 1, 2011
Guidance Regarding DAIDS Deregistration Process
September 30, 2011
Proper Handling of Confidential Documents
September 22, 2011
Home
|
About the RSC
|
Frequently Asked Questions
|
Contact Information
|
Useful Links
|
Secure Document Collaboration Site
|
Broadcast Memos
|
DAIDS RSC Presentations
Regulatory Information
|
Human Subjects Protection
|
Protocol Development Information
|
Protocol Registration
|
Safety and Pharmacovigilance
|
Case Report Form Management
Copyright © 2011 DAIDS RSC. All rights reserved. |
Accessibility
|
Privacy Policy
|
Disclaimer