2026 GMS5003 Fundamentals of Health Products Regulation

The regulation of health products relies on standards, guidelines, and legal frameworks. Effective governance, ensuring timely access to safe, high-quality, and effective medicines for patients, depends on collaboration among stakeholders including the industry, regulatory authorities, healthcare professionals, and patients.

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

This course explores the roles and contributions of various stakeholders, key functions, and guidelines that shape today’s regulatory landscape. You will gain comprehensive insights into the end-to-end processes of pharmaceutical development, learning how regulatory requirements apply across the entire product lifecycle, enabling you to navigate contemporary regulatory challenges and contribute effectively to product development and compliance strategies.

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