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Difference between revisions of "Regulated Clinical Research Information Management"
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*[[Structured_Product_Labeling]] | *[[Structured_Product_Labeling]] | ||
| − | [[ | + | ==Working Group Meetings== |
| + | [[RCRIM Working Group Meeting Agendas]] | ||
Revision as of 15:16, 14 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
