Medical devices
10 EU MDR compliance experts
These ten medical device professionals have held EU MDR compliance roles inside manufacturers, from running MDR programs and projects to serving as the Person Responsible for Regulatory Compliance. A reader can learn how device companies organize and carry out EU MDR compliance work.
Professionals to explore
01—10Agnes David
LinkedInExperience: EU MDR Project Manager (TechFiles) · Johnson & Johnson
EU MDR Project Manager (TechFiles) at Johnson & Johnson since November 2018, a role the profile places at DePuy Synthes Companies (J&J). The profile says the role leads DePuy Synthes supply chain compliance activities for external manufacturing compliance to MDR. Other listed roles include Project Manager at MedRes Group (2014–2018) and NPI (New Program Introduction) at Flex (2013–2014).
Begoña Patron
LinkedInExperience: PRRC MDR and Switzerland · Abbott Medical
PRRC MDR and Switzerland at Abbott Medical since June 2021, alongside the role of Regulatoy Compliance & Quality System Manager South Europe there since 2019. Duties the profile lists for the PRRC role include checking the conformity of medical devices before the devices are released and making sure post-market surveillance obligations are met. The listing also shows Tecnico Responsable Abbott Medical España at Abbott Medical España SA since 2018.
Daniel Cser
LinkedInExperience: Person Responsible for Regulatory Compliance (EU MDR) · Mediso Medical Imaging Systems
Person Responsible for Regulatory Compliance (EU MDR) at Mediso Medical Imaging Systems since May 2021, alongside the role of Quality Director there since 2018. The profile cites experience with the transition to (EU) 2017/745 (MDR), clinical evaluation under MEDDEV 2.7.1 v4, and EU MDR and US FDA UDI implementation. Other listed roles at the company include Quality Manager (2012–2018) and Quality Project Leader (2005–2011).
Dorian Müller‐Borges
LinkedInExperience: Regulatory Affairs Specialist (MDR Transition) · Curasan AG
Regulatory Affairs Specialist (MDR Transition) at Curasan AG since April 2026, where the profile describes preparing and maintaining MDR Technical Documentation for multiple medical devices in accordance with Regulation (EU) 2017/745 and developing retrospective design and development documentation. Other listed roles include Head of Quality Management at NovaCutis GmbH (2025–2026) and Quality Manager at NovaCutis GmbH (2024–2025).
Douglas Raymond
LinkedInExperience: R&D Director, EU MDR Implementation - Program Lead · Johnson & Johnson MedTech
Former R&D Director, EU MDR Implementation - Program Lead at Johnson & Johnson MedTech (2018–2025), and R&D Director, EUMDR & Eudamed Implementation, Program Lead J&J MedTech Orthopaedics (2024–2025). The profile describes leading end-to-end R&D programs and driving regulatory compliance with EU MDR and EUDAMED. Since August 2025 the listing shows R&D Director, Strategy & Operations, Systems Transformation at the same company.
Helene Wilson, JD, PMP, CQE, CMQ
LinkedInExperience: EU MDR Program Manager · Integra LifeSciences
EU MDR Program Manager at Integra LifeSciences since March 2022; the profile describes Integra LifeSciences as a medical equipment manufacturing company. Other roles in the listing include Project Manager at Ethicon, Inc. (2019–2021) and Project Attorney at UnitedLex (2019). The profile lists JD, PMP, CQE and CMQ credentials with the name.
Peter Dekempeneer
LinkedInExperience: RA -Director EU MDR for Regulatory Compliance · Philips
RA -Director EU MDR for Regulatory Compliance at Philips since June 2019. The profile places the role in the EU Authorized Representative organization, ensuring correct execution of the EU Authorized Representative mandate and the compliance of non-EU businesses with the European New Legislation Framework. Other listed roles include Head of Quality Assurance & Regulatory Affairs International at Philips Volcano (2016–2019).
Ralf Schmidt
LinkedInExperience: Commercial Quality Lead and EU MDR Person Responsible for Regulatory Compliance · Kenvue
Commercial Quality Lead and EU MDR Person Responsible for Regulatory Compliance at Kenvue since May 2023. In this role, the profile says, the work includes leading the EMEA Legal Manufacturer Quality & Compliance organization. The listing shows only this one work row, so it does not cover the rest of the career history.
Stephanie Butler
LinkedInExperience: Sr. Program Manager - EU MDR Compliance · Medtronic
Sr. Program Manager - EU MDR Compliance at Medtronic since August 2026, and Sr. Engineering Program Manager (CTOR) at Medtronic from 2022 to 2026. The profile describes a program management leader for cross-functional initiatives across medical devices, product development, manufacturing and regulatory compliance. Other listed roles include Director of Manufacturing - Personal Cancer Monitoring at Invitae (2020–2022).
Yvonne Hug
LinkedInExperience: Senior Regulatory Affairs Manager · Sensile Medical AG a Gerresheimer Company
Former Senior Regulatory Affairs Manager at Sensile Medical AG a Gerresheimer Company (2024–2026), a role in which the profile says regulatory strategy and documentation were led for the MDR 2017/745 submission and approval of a programmable infusion pump for Parkinson's therapy, with Notified Body interactions coordinated. Also Regulatory Affairs Manager at Sensile Medical AG (2019–2024) and Senior Regulatory Affairs Manager at RMS Foundation since January 2026.
Choose the right perspective
Match the person's seat to your question, since running an MDR transition program, preparing technical files and acting as the Person Responsible for Regulatory Compliance involve different day-to-day work. Also weigh company size and product range, because a large multi-portfolio manufacturer faces different MDR tradeoffs than a smaller company with a few device families.
Questions to take into the conversation
- 01How did you plan and prioritize moving an existing device portfolio from the old directives to EU MDR?
- 02What did notified bodies push back on most in your technical documentation, and how did you respond?
- 03How do you set up the Person Responsible for Regulatory Compliance role and post-market surveillance so they hold up in an audit?
Reaching EU MDR compliance experts
How can I contact one of these EU MDR compliance experts?
Pick one of the 10 people on this page and choose "Book a paid call", or describe your project to find others. You offer a fee for a 15-minute call or a written answer, Instant Expert finds the person's work email and sends the invitation, and they decide whether to accept. The list covers 10 companies, including Johnson & Johnson, Abbott Medical and Mediso Medical Imaging Systems, based on profile data retrieved on October 3, 2026. Being listed here doesn't mean someone has agreed to take calls.
How much does it cost to reach EU MDR compliance experts?
You choose the offer, starting at $5 per person. It includes Instant Expert's 20% fee, so an offer that pays the person $100 costs you $125. You're charged only when the person books the call or sends the answer.
What if they don't reply?
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About this directory
This is a professional research starting point based on business profile data retrieved on . Titles and companies reflect that source snapshot and may describe past or present roles. Check the linked profiles for current details. Inclusion does not imply Instant Expert membership or availability.
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