EU HTA Regulation: What It Means for Medtech and IVD Market Access Webinar
Learn how the upcoming EU HTA regulation could reshape market access for Medtech and IVD companies.
The new EU HTA framework is set to bring significant changes in how medical devices and diagnostics are evaluated across Europe. While many details are still being finalized, this webinar offers early insights based on current developments and practical experience.
Join us to explore what’s ahead, how national decision-making might be affected in key markets like Germany and France, and what steps your company can take now to prepare.