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Guidance Documents/Guidance-Document/Data Retention When Subjects Withdraw from FDA-Regulated Clinical Trials: Guidance for Sponsors, Clinical Investigators, and IRBs

Data Retention When Subjects Withdraw from FDA-Regulated Clinical Trials: Guidance for Sponsors, Clinical Investigators, and IRBs

Detailed guidance document from FDA and regulatory agencies.

Document Details

Guidance Document

October 1, 2008

July 21, 2021

Office of the Commissioner

3358ed6a-403d-4aaa-b66c-941d2d2630ab

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