🎥 Recordings Available - SBIA | Good Clinical Practice & Pharmacovigilance Compliance Symposium

U.S. Food and Drug Administration sent this bulletin at 04/08/2024 10:00 AM EDT

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FDA | CDER | Small Business and Industry Assistance (SBIA)

 

A Joint US-FDA | MHRA-UK | Health Canada Good Clinical Practice & Pharmacovigilance Compliance Symposium

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Recordings are now available to view and/or share with colleagues.

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🔹 ABOUT THIS WEBINAR:

This workshop focused on Global Clinical Trials in Good Clinical Practice, Bioequivalence, and Pharmacovigilance in the post pandemic world. Presentations and panel discussions provided information on the recent updates made to ICH E6(r3) and regulatory perspectives on implementation of proportionate and risk-based approaches to the design and conduct of the trial to help ensure that the quality of the trial data generated is of sufficient quality to support good decision making.

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