2026 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 explores the regulatory frameworks, clinical evaluation processes, and risk management strategies essential for the development and approval of medical devices. You will be provided a detailed understanding of preclinical testing, clinical evidence generation, and post-market surveillance, highlighting best practices for ensuring device safety and performance.

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