Stay current. Strengthen compliance. Enhance participant safety.

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Who should Attend

This practical half-day workshop is designed for clinical research professionals who want to refresh their pharmacovigilance knowledge and stay up to date with the latest regulatory expectations, safety reporting requirements, and current best practices.

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Description

The session will cover the core principles of pharmacovigilance across the clinical trial lifecycle. Using practical examples, and discussions of common inspection findings, the workshop reinforces the critical aspects of adverse event reporting, safety oversight, and the respective responsibilities of investigators, sponsors, and study teams.

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Aims

By the end of the session, delegates will be able to confidently apply current pharmacovigilance requirements in their day-to-day clinical research activities, strengthen regulatory compliance, and contribute to the protection of trial participants.

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Ideal for: Clinical research professionals seeking a practical update on pharmacovigilance and safety reporting, whether returning to the topic or looking to reinforce existing knowledge.