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Clinical Trials Transformation Initiative

Optimizing Expedited Safety Reporting for Drugs and Biologics Subject to an Investigational New Drug Application

Posted on November 7, 2013February 11, 2025 by Hannah Faulkner

Optimizing Expedited Safety Reporting for Drugs and Biologics Subject to an Investigational New Drug Application

This entry was posted in Publications, Related: Safety Reporting, SAE Reporting, Safety, Safety Reporting, Study Operations. Bookmark the permalink.

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