Clinical & Post-Marketing Safety Training Course

This two-day course provides a comprehensive, practical introduction to international standards and best practices in drug safety monitoring across the full product lifecycle.

Covering both clinical and post-marketing pharmacovigilance, the course explores how safety data is captured, assessed, and reported in line with global ICH guidelines. You’ll build a clear understanding of adverse event reporting, safety signal detection, and risk management - from early development through to real-world use.

The course also examines how safety information is communicated and maintained within key regulatory documents, alongside the evolving expectations placed on organisations to monitor and manage product risk effectively.

Designed to bridge theory and real-world application, this training equips you with the knowledge and confidence to navigate regulatory requirements, support compliance, and contribute to robust safety systems within clinical and post-authorisation settings.