search
Englishexpand_more
No other languages available
Contact us
search
ENG
No other languages available for now
Contact us
Blog Hero
Event

Meet and Greet Gert Bos and Oliver Schaer at the MedTech Summit 2026

Join us at the MedTech Summit in Berlin. Attend Gert Bos' panel discussion on balancing risk and patient safety (in the wake of EU MDR/IVDR revisions) and network with Oliver Schaer on-site.

Date: 15-18 June 2026

Location:  JW Marriott Hotel Berlin, Germany

Introduction:

The MedTech Summit, organised by Informa Connect, is one of Europe’s leading events for medical device and IVD regulatory affairs, compliance, and innovation. Bringing together regulators, Notified Bodies, industry leaders, and MedTech professionals from across the globe, the summit focuses on the latest developments in MDR, IVDR, AI in healthcare, software as a medical device (SaMD), clinical investigations, post-market surveillance, and global market access strategies.

The event offers a unique opportunity to gain practical insights into the rapidly evolving regulatory landscape while learning directly from experts shaping the future of the MedTech industry. Exchange knowledge, explore emerging trends, and build valuable industry connections through keynote sessions, panel discussions, and networking opportunities. With regulatory changes and technological innovation moving faster than ever, the MedTech Summit focuses on staying ahead, strengthening compliance strategies, and driving innovation within organizations.

Meet and greet Gert Bos and Oliver Schaer at the MedTech Summit. Gert Bos will participate as a speaker in a panel discussion (see details below), while Oliver Schaer will also be attending the event on-site. Both look forward to connecting with fellow attendees, exchanging insights, and network throughout the summit. 

Session details:

| 11:40 - 12:25 CEST

Panel Discussion Topic:  'Balancing Risk and patient Safety: Redefining Risk Acceptance in the Wake of EU MDR/IVDR Revisions

  • Examining how EU MDR/IVDR revisions are reshaping the definition of risk acceptance in medical device and IVD development.
  • Adapting to change - providing actionable insights for manufacturers to align risk management practices with the new regulatory expectations.

For more details, visit the event website.