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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. 

How the GMS5003 Fundamentals of Health Product Regulation can benefit your career

This fundamental course will provide you with an understanding of the role of various stakeholders, functions, and guidelines that shape the regulatory environment and influence the healthcare management landscape. You will explore the concept of the product life cycle, along with other contemporary regulatory approaches, helping you gain a comprehensive view of how regulations impact healthcare systems.

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

v1 Flyer_2025 GMS5003 Fundamentals of Health Products Regulation

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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