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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. 

This course describes the unique approaches for the product design and development, as well as regulation of medical devices and technology. Key concepts for assessing the clinical performance of medical devices will be introduced, facilitating the understanding of an optimal environment for health technology adoption.

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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