MedTech Summit

Event Information

Join 500+ medical device, diagnostics and combination product experts in Brussels on 17-21 June 2018 to hear about the latest updates, insights and implementation strategies surrounding the EU MDR, IVDR and Emerging Market regulations. Plus, hear from 15+ Competent Authority & Notified Body representatives alongside lots of industry case studies for direct perspectives from these key stakeholders.

Build your 2, 3, 4 or 5 day pass to benefit from the 9 streams and 2 training courses covering: - EU Medical Device Regulation (Days 1 & 2) - 17-18 June 2019 - EU Medical Device Law (Days 1 & 2) - 17-18 June 2019 - Clinical Evaluations & Investigations (Days 2 & 3) - 18-19 June 2019 - Post Market Surveillance & Vigilance (Days 2 & 3) - 18-19 June 2019 - TRAINING COURSE: Medical Device Regulatory Project Management (Day 3) - 19 June 2019 - Medical Device Regulatory Affairs in Emerging Markets (Days 3 & 4 & 5) - 19-21 June 2019 - Clinical Outsourcing (Day 4) - 20 June 2019 - TRAINING COURSE: US Regulatory Affairs for Medical Devices (Day 4) - 20 June 2019 - EU IVD Regulation & Strategy (Days 4 & 5) - 20-21 June 2019 - Drug Device Combination Products (Days 4 & 5) - 20-21 June 2019 - Sterilisation & Reprocessing (Day 5) - 21 June 2019 Visit the website to find out more!