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2025 GMS5003 Fundamentals of Health Products Regulation

Regulation of health products is controlled by standards, guidelines and legal frameworks. The interactions among these and the stakeholders – industry, regulatory authorities, healthcare professionals and patients – are required for effective governance for timely access and safe, quality and efficacious medicines and medical devices for patients. 

This fundamental course provides the understanding of the contribution of the various stakeholders, functions and guidelines that shape the regulatory environment and impact the healthcare management scene. The concept of product life cycle will be also be explored among other contemporary regulatory approaches. 

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

Flyer_2025 GMS5003 Fundamentals of Health Products Regulation - with stamp

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

   


Date and Time


27 Oct 2025 @ 08:30 - 31 Oct 2025 @ 17:30

Speaker


 

Venue


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