Clean and standardize clinical trial data to CDISC SDTM standards for FDA/EMA regulatory submissions. Handles missing values, outlier detection, date standardization, and generates audit trails for DM, LB, and VS domains.
92
91%
Does it follow best practices?
Impact
Pending
No eval scenarios have been run
Passed
No known issues
Loading evals
ca9aaa4
If you maintain this skill, you can claim it as your own. Once claimed, you can manage eval scenarios, bundle related skills, attach documentation or rules, and ensure cross-agent compatibility.