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Regulated Clinical Research Information Management
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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
