Live MedPharmPlast Europe Webinar 6 April 2022

Save the Date and Register Now!

MedPharmPlast Europe (MPPE) and Polymer Comply Europe (PCE) are pleased to invite you to their next live webinar on the 6th of April 2022 between 10.00 - 11.00 CET.

Agenda:

  • Welcome & Introduction by Moderator ​
    Nigel Talboys, Terumo, MPPE Regulatory Task Force Chair
  • Update concerning Borderline and Classification under MDR
    Paul Piscoi, Scientific Policy Officer, European Commission
  • Live Questions & Answers 
  • Closing

Registration:

Participation is free of charge, registration is required.

Meet the Speaker

Paul Piscoi graduated as a medical doctor and has been working at the European Commission for more than 13 years. Since February 2012, he has worked as a Policy and Scientific Officer in the Unit dealing with medical devices (currently Unit B.6 of the Directorate-General for Health and Food Safety). Besides the participation in the drafting of implementation acts related to the new Medical Devices Regulations and other tasks, he is responsible for the coordination of the Clinical Investigation and Evaluation Working Group, the Borderline and Classification Working Group, vigilance and scientific matters.

 

 

 

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About MedPharmPlast Europe

MedPharmPlast Europe is a sector group of EuPC created in 2014 by and for companies involved in the whole supply chain of plastic medical devices and pharmaceutical packaging in Europe. It assists companies in these industry sectors by keeping them informed about the latest developments in European regulations and their impact on the medical device and pharmaceutical packaging plastics value chain. MedPharmPlast Europe also represents the interests of the industry to the European legislators and tries to arrive at regulations that are both workable and protect the patient.

Contact

Avenue de Cortenbergh 71 1000 Brussels Belgium

+32 (0)2 739 63 88

[email protected]

www.medpharmplasteurope.org