Conference Description:

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 11-15 June 2018, 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 & Investigations for Medical Devices
- Post Market Surveillance & Vigilance
- Medical Device Regulatory Affairs in Emerging Markets
- IVD Regulation & 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.

For sponsorship and exhibition opportunities please contact Linda Cole: E. [email protected]

Brochure https://go.evvnt.com/203219-0?pid=154
Booking https://go.evvnt.com/203219-1? pid=154

Prices:
2 Day Pass: GBP 1899
3 Day Pass: GBP 2499
4 Day Pass: GBP 2799
5 Day Pass: GBP 3199

Speakers: Gert Bos, Bassil Akra, Arnd Hvoeler, Perta Kaars-Wiele, Stephen Lee, Elizabeth Gfoeller, Wen Pang, Itoro Udofia, Pamela Barrows

Time: on Monday June 11, 2018 at 8:50 am (ends Friday June 15, 2018 at 4:55 pm)