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ADaM defines dataset and metadata standards that support:
- efficient generation, replication, and review of clinical trial statistical analyses, and
- traceability among analysis results, analysis data, and data represented in the Study Data Tabulation Model (SDTM).
ADaM is one of the required standards for data submission to FDA (U.S.) and PMDA (Japan).
ADaM Blended (PRIVATE TRAINING ONLY)
Zoom + Online (self-paced)
3 weeks: On-Demand modules + 1-hour virtual Q&A session per week