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Markus Pöttker
MDR Post Market Surveillance Lead at Smith & Nephew


Markus spent four years in Quality & Regulatory roles, before becoming the Director of Complaint Management and Head of Regulatory Compliance at Smith + Nephew with global responsibility for Complaint Handling, Medical Device Reporting and interaction with Regulatory Agencies. Since April 2018, he is a member of the EU MDR Global Project team leading the Post Market Surveillance work stream at Smith + Nephew and is responsible for ensuring that the requirements of the EU MDR are correctly interpreted, specified and implemented across the business functions globally. Markus has been a member of the MedTech Europe PMS & Vigilance Working Group since 2012 and is a member of the corresponding standard committee to ISO TC 210 at the Swiss Association for Standardization. Markus holds a masters degree in law from WWU Münster, Germany.

Agenda Sessions

  • Manufacturer’s Experience Meeting PMS Requirements

  • Manufacturer Q+A