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Difference between revisions of "Regulated Clinical Research Information Management"
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| − | [[ | + | *CDISC Content to Message [[Study_Design%2C_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]] | |
| − | [[ | ||
| − | |||
| − | [[ | ||
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| − | [[ | ||
Revision as of 16:46, 13 October 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
