Current course offerings

Please Note: Course profiles marked as not available may still be in development.

Course description

This course covers medicines regulation, clinical trial phases, designs and protocol development, along with trial governance, monitoring and audit. You will gain a comprehensive knowledge of Good Clinical Practice (GCP), the clinical and regulatory aspects of drug development, and the significance of risk management. You will also recognise the importance of the regulations in ensuring appropriate biometric data management and transparency of the drug development process.

Archived offerings