This site is part of the Informa Connect Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.

15 - 17 June 2021
Virtual EventDelivered in CEST time zone

Markus Pöttker
MDR Post Market Surveillance Lead at Smith & Nephew


Markus is a member of the EU MDR Project team at Smith&Nephew leading the Post Market Surveillance work stream. In this role, he is responsible that the requirements of the EU MDR are correctly interpreted and implemented across all. Prior to this, he spent seven years in Quality & Regulatory roles, at last he was the Director of Complaint Management and Head of Regulatory Compliance with global responsibility for Complaint Handling, Medical Device Reporting and interaction with Regulatory Agencies. Markus is co-chair of MedTech Europe PMS & Vigilance Working Group and a member of the corresponding standard committee to ISO TC 210 at the Swiss Association for Standardization. Markus holds a master’s degree in law from WWU Münster, Germany.

Agenda Sessions

  • Manufacturer’s Experience Meeting PMS Requirements

  • Manufacturer Q+A