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Workshop: The new EU Medical Device & in-vitro Diagnostic Regulations


  • Stendard 71 Ayer Rajah Crescent, #02-01 Singapore, 139951 Singapore (map)

Stendard, together with TÜV Rheinland and MT Promedt Consulting GmbH, is organising the first-ever tripartite workshop! Come and get first-hand updates on the new Medical Device Regulation (MDR) and in-vitro Diagnostic Regulation (IVDR), what are Notified Bodies looking out for during the audits and how you can leverage on software to help you transit your products from the current directives to the new regulations.

Singapore companies eligible for PIC are able to claim 40% off post-discounted tickets. Register now with discount code "IAMEARLY" for attractive early-bird discount!


About the MDR & IVDR Implementation
As mentioned, the new European Medical Devices Regulation (MDR) and in-vitro Diagnostics Regulation (IVDR) have been finalised and published in the Official Journal of the European Union, as Regulation 2017/745 and 2017/746 respectively. The Regulations will enter into force on 25 May 2017, marking the start of the transition period for companies selling medical devices into Europe.
 
How to get your organisation ready?
We are excited to announce that we have organised a two full-days’ workshop, not only just focusing on the MDR & IVDR updates, but we will also be discussing on the possible implementation strategies for your organisation!

Guest Speakers: 
Dr Michael Rinck (MT Promedt Consulting GmbH, Germany)
Mr Clemens Mohr (MT Promedt Consulting GmbH, Germany)
Ms Jocelyn Reyes (TÜV Rheinland, Singapore)
Mr Jason Lim (Stendard, Singapore)
 
For more information about the workshop schedule, the discussion topics and registering for the workshops, please click the button below:
 

Earlier Event: May 17
Tech in Asia Singapore 2017