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Do not miss the opportunity to participate at the 2017 PROSYSTEM Symposium in Zurich, Switzerland.

PROSYSTEM will introduce the latest up-dates on the new legal requirements at our SYMPOSIUM in Zurich. This Symposium focuses on the implementation of the new requirements for Medical Device manufacters and other “economic operator” and higlights the major changes. The invited speakers from BSI will represent the perfectives of a Notified Body under the new regulations MDR and IVDR.

Cutting-edge issues:

  • Current status of Negotiation & New Content of the MDR
  • Future roles of Notified Bodies & supervision by the EU
  • MDR Quality Management System Requirements & ISO 13485:2016
  • Clinical Evaluation & Clinical Investigation for Medical Devices
  • The new IVD Regulation

Download full agenda

Our evening get together on day 1 with appetizers and drinks provides the opportunity for networking and interchange of ideas.
Sign up today for a place at the PROSYSTEM symposium and benefit from being part of the expert discussion. Our evening drinks reception and dinner will give you the opportunity to network with your colleagues.

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