MedTech Summit

Join 300+ medical device and IVD professionals at the MedTech Summit to get crucial EU MDR and IVDR guidance as well as emerging market regulatory advice from the Competent Authorities, Notified Bodies and Industry. The comprehensive agenda covers 8 key areas to make sure your have all the information you need to ensure fast and effective compliance including:

- EU Medical Device Regulation (Days 1 & 2)
- EU Medical Device Law (Day 1)
- Clinical Evaluations & Investigations for Medical Devices (Days 2 & 3)
- Post Market Surveillance and Vigilance (Days 2 & 3)
- Medical Device Regulatory Affairs in Emerging Markets (Days 3 & 4 & 5)
- Companion Diagnostics (Day 3)
- IVD Regulatory and Strategic Forum (Days 4 & 5)
- Drug Device Combination Products (Days 4 & 5)

Visit the website to find out more: lifesciences.knect365.com/medtech-summit