Module 2 Overview of Annex 22

EU GMP Annex 22 establishes regulatory expectations for the use of Artificial Intelligence in pharmaceutical quality systems and manufacturing processes. In this module, explore the scope, objectives, key requirements, and compliance principles outlined in Annex 22 to support the effective and compliant use of AI in GxP environments.

Видео Module 2 Overview of Annex 22 канала WhitehallTraining