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2025 GMS5108 Clinical Studies and Evaluation of Health Products

The effective regulation of pharmaceuticals and medical devices for safety and efficacy depends on the availability, understanding and appropriate implementation of relevant guidelines and the processes designed to ensure quality in decision-making. The requirements are frequently different from traditional clinical trials and specific to regulatory affairs.

This course provides the understanding for the unique requirements of clinical trials and clinical data meant to support regulatory evaluation and approvals. 

Due to the limited availability of seats, early registration is strongly recommended.

Flyer_2025 GMS5108 Clinical Studies and Evaluation of Health Products

Click here for a step by step guide on how to register.

  


Date and Time


24 Mar 2025 @ 08:30 - 28 Mar 2025 @ 17:30

Speaker


 

Venue


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