Vendor Showcase – Navigating Regulatory Changes for Packaging & Labeling: Lessons Learned From the Transition to the EU Clinical Trial Regulation – Hosted by Clinigen

The transition from the Clinical Trial Directive to the EU Clinical Trial Regulation has created significant operational challenges for clinical trial supplies.

This session will discuss Clinigen’s proactive approach to managing the regulatory change for packaging and labelling to ensure seamless compliance.

This included a comprehensive impact analysis, client education initiatives and tailored solutions to reduce complexity and avoid delays.

You will learn best practices for navigating change and gain insight into how you can mitigate risk and maintain operational excellence.

Presented by: Mélany Pierard, Project Manager, Team Lead, Clinical Supply Management & Mathieu Denis, Project Manager Solutions, Clinical Supply Management