Legal experts from Taylor Wessing provide a deep dive into the amendments to the EU MDR and IVDR regulations, covering the proposed changes, transition timelines, and practical implications for medical device manufacturers.
By Dr. Hatem Rabeh · Published April 7, 2026
Legal experts from Taylor Wessing provide a deep dive into the amendments to the EU MDR and IVDR regulations, covering the proposed changes, transition timelines, and practical implications for medical device manufacturers.
The comprehensive free database for medical device companies, FDA-cleared devices, EU Notified Bodies, competent authorities, clinical guidelines, and regulatory resources worldwide — 4,975 companies · 5,064 devices · 53 EU Notified Bodies · 1,129 resources & guidelines. Founded by Dr. Hatem Rabeh (MD, MSc Ing).