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| − | [[Main Page]] | RCRIM | + | [[Main Page]] | '''Regulated Clinical Research Information Management (RCRIM)''' |
This page is for the RCRIM TC | This page is for the RCRIM TC | ||
Revision as of 20:08, 12 December 2008
Main Page | Regulated Clinical Research Information Management (RCRIM)
This page is for the RCRIM TC
Contents
RCRIM projects include:
- CDISC Content to Message Study_Design,_Study_Participation_and_Subject_Data
- Clinical_Trials_Registration_and_Results
- Drug Stability Reporting
- Laboratory Result-based Adverse Event Assessment Messaging Project
- Medical Product and Device Listing
- Periodic Reporting of Clinical Trial Laboratory Data, Release 2
- Regulated Product Submissions
- Structured_Product_Labeling
Working Group Meetings
RCRIM Working Group Meeting Agendas
Meeting Minutes
RCRIM Working Group Meeting Minutes
Decision Making
see Work Group Decision Making Documents[1]
Reference Links
BRIDG file release site http://gforge.nci.nih.gov/frs/?group_id=342
BRIDG Project site http://gforge.nci.nih.gov/projects/bridg-model/
