All Events

Back

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.

How the GMS5108 Clinical Studies and Evaluation of Health Products can benefit your career

This course will provide you with an understanding of the unique requirements for clinical trials and clinical data that support regulatory evaluation and approvals. You will learn how to navigate the processes involved in ensuring clinical data meets the necessary standards for regulatory success.

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

V2 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


Browser not supported

Modern websites need modern browsers

To enjoy the full experience, please upgrade your browser

Try this browser