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2025 GMS5008 Regulation and Clinical Evaluation of Medical Devices

Health products cover a wide spectrum of modalities, ranging from pharmaceuticals, biologics to medical technology. The regulatory frameworks and requirements differ between medical technology and the others. 

How the GMS5008 Regulation and Clinical Evaluation of Medical Devices can benefit your career

This course will describe the unique approaches to product design, development, and regulation of medical devices and technology. You will be introduced to key concepts for assessing the clinical performance of medical devices, helping you understand how to create an optimal environment for the adoption of health technology.

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

v2 Flyer_2025 GMS5008 Regulation and Clinical Evaluation of Medical Devices - with stamp

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


Date and Time


07 Jul 2025 @ 08:30 - 11 Jul 2025 @ 17:30

Speaker


 

Venue


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