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Difference between revisions of "Regulated Clinical Research Information Management"
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[[Regulated Product Submissions]] | [[Regulated Product Submissions]] | ||
| − | [[Study_Design%2C_Study_Participation_and_Subject_Data]] | + | CDISC Content to Message [[Study_Design%2C_Study_Participation_and_Subject_Data]] |
[[Structured_Product_Labeling]] | [[Structured_Product_Labeling]] | ||
[[Clinical_Trials_Registration_and_Results]] | [[Clinical_Trials_Registration_and_Results]] | ||
Revision as of 16:09, 13 October 2008
Main Page | RCRIM
This page is for the RCRIM TC
RCRIM projects include:
Laboratory Result-based Adverse Event Assessment Messaging Project
CDISC Content to Message Study_Design,_Study_Participation_and_Subject_Data
