MedTech Summit is organized by KNect365 Life Sciences and will be held during Jun 11 - 15, 2018 at Hotel NH Brussels Bloom, Brussels, Belgium.
With the EU MDR and IVDR transition periods flashing before our eyes, alongside on-going global regulatory updates, now is the time to ensure you have the strategies and resources in place to meet these key compliance deadlines.
On this conference, 450 medical device, diagnostics and combination product experts will be gathering in Brussels at the MedTech Summit to discuss the latest regulatory updates, expectations, and challenges across 8 key areas:
• EU Medical Device Regulation.
• EU Medical Device Law.
• Clinical Evaluations and Investigations for Medical Devices.
• Post Market Surveillance and Vigilance.
• Medical Device Regulatory Affairs in Emerging Markets.
• IVD Regulation and Strategy and Companion Diagnostics.
• Drug Device Combination Products.
• Sterilisation and Reprocessing of Medical Devices.
With direct feedback from the EU Commission, 25 Competent Authority and Notified Body representatives, and Industry, make the most of the opportunity to ask your questions, benchmark and get the practical advice you need to help you along the path to compliance.
Additional details will be posted as soon as they are available.