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Do not miss the opportunity to participate at the 2016 PROSYSTEM Symposium in Milpitas, CA.

This time, the focus lies on the new Medical Device Regulation (MDR). Within the next 6 month the translations of the MDR text into 23 other official EU languages needs to be a presented to the EU-member States, EU Parliament (and EU commission) for their final political votes. The MDR will come 21 days after publication into force.

Cutting-edge issues:

  • New rules for ‘economical operator’
  • Traceability for clinical data
  • Stricter vigilance & post-market surveillance
  • New rules for Notified Bodies

Download full agenda

Our evening get together on day 1 with appetizers and drinks provides the opportunity for networking and interchange of ideas.
As an active member of several standardization groups we provide you with upcoming new standards and their proper implementation. Our speakers are international standardization experts and will update you with inside knowledge to prepare you for the challenges the medical device industry faces in 2016 and 2017. Discuss your questions and concerns during the tracks or offsite with the speakers and other participants.

Do not miss the chance and be part of our PROSYSTEM Symposium! GET IN TOUCH WITH SOLUTIONS!

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