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EU Medical Device Regulation:
Immediate Actions to Meet Your 2020 Deadline

Two-part MDR Series: Stay for One, or Both

When: Tuesday, June 11 | 3:00 pm - 4:00 pm 
Where: Room 49 - Product Lifecycle Management Track
Level: Intermediate, Advanced
Participant Type: Research & Development, Product Development, Regulatory/Clinical Affairs, Sales & Marketing, Supply Chain Management, Quality Control



In light of the looming May 2020 compliance deadline for the EU Medical Device Regulation (MDR), TÜV SÜD will review the regulation’s core changes, share the main challenges that orthopedic device manufacturers face and leave adequate time for you to pose questions to a Notified Body. MDR is expected to have a significant impact within multiple departments of device companies. This session is intended to provide answers to your pressing questions and a check list of actions to take in the final months of the transition period.

Attendee Takeaways

  • Learn the challenges that orthopedic manufacturers face with MDR compliance
  • Recieve a basic overview of the Medical Device Regulation
  • Benefit from a face-to-face Q&A with a Notified Body


Max Singh, Ph.D., is Global Director – Orthopedic Focus Team, TÜV SÜD Product Service. Dr. Singh joined TÜV SÜD in July 2017. Previously, he spent 15 years in the medical device industry, working primarily at orthopedic manufacturers including KARL STORZ, Stryker and ulrich medical. Amongst other responsibilities, Dr. Singh held R&D positions that led the design of high-risk orthopedic devices. Dr. Singh studied medical engineering and business administration, and holds a Ph.D. in economic sciences.


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