Medical Device Development & Case Presentation workshop held at SUNUM on March 4, 2026, provided valuable insights into the European Medical Device Regulation (EU MDR) and In Vitro Diagnostic Regulation (IVDR) frameworks, which are critical for anyone involved in medical device research, development, or commercialization in the European market. Participants also engaged in hands-on group work through a real-world case study presentation.
The workshop delivered by Dr. Bahar Bingöl, Scientific Senior Consultant – Emendo Research and Development (Denmark) was open faculty, researchers, and graduate students.
