Lead organizational change to ensure clinical and regulatory processes are compliant with EU IVDR. Global regulatory stakeholders clarify guidance and best practices to demonstrate real-life product efficiency, including executing clinical trials that garner sufficient evidence. Exchange lessons learned in preparing technical files and benchmark appropriate budget and resource allocation with peers.
Foster a sense of collaboration and safely connect with peers and expert presenters at this intimately-sized program. Customize your experience and address your unique concerns during dynamic Q&A after each session. Our commitment to industry perspectives keeps the program focused on what matters and dynamic session formats allow you to stay engaged.