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Difference between revisions of "Regulated Clinical Research Information Management"
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==Working Group Meetings== | ==Working Group Meetings== | ||
[[RCRIM Working Group Meeting Agendas]] | [[RCRIM Working Group Meeting Agendas]] | ||
| + | |||
| + | ==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/ | ||
Revision as of 18:19, 20 November 2008
Main Page | RCRIM
This page is for the RCRIM TC
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
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/
