CoMeCT Workshop: Breaking Barriers in Regulatory Approvals
Regulatory approval remains one of the most complex and time-consuming steps in conducting multi-arm, adaptive clinical trials and master protocols. As these innovative trial designs become increasingly common, it is essential to ensure that regulatory processes evolve accordingly, fostering efficiency while maintaining scientific and ethical rigor.
To address these challenges, CoMeCT is organising a dedicated workshop: Breaking Barriers: Streamlined Approvals for Multi-Arm, Adaptive Clinical Trials and Master Protocols.
This 90-minute session will bring together regulators, national competent authorities, clinical researchers, and trial methodologists to exchange on best practices, lessons learned, and future directions.
What to expect
Participants will gain insights from real-world use cases, including major European platform trials, and hear directly from national competent authorities and the European Medicines Agency (EMA). The event will conclude with a dynamic panel discussion bringing together diverse perspectives on how to improve approval and amendment processes for complex trials.
The detailed agenda and speaker list will soon be available on this page.
Why attend?
- Learn from leading experts and regulators
- Explore solutions to streamline approval processes
- Connect with peers shaping the future of complex trials in Europe
Registrations are now open!
Secure your spot and be part of the conversation.