Emergo by UL Webinar: FDA QMSR Changes – Compliance Steps for Medical Device Manufacturers
Expert-led webinar on FDA QMSR changes and the compliance steps medical device manufacturers need to take before the 2026 deadline. […]
Expert-led webinar on FDA QMSR changes and the compliance steps medical device manufacturers need to take before the 2026 deadline. […]
Free webinar covering practical design control processes for medical device development, including design inputs, outputs, verification, and validation under FDA
MedTech Europe webinar combining regulatory context with practical operational guidance for EUDAMED UDI registration ahead of the May 28, 2026
BSI notified body experts discuss the regulatory requirements and transition timelines for Class C IVD device manufacturers under the EU
Qserve regulatory experts analyze the proposed EU MDR and IVDR revision (MDR 2.0), covering changes to software classification, AI Act
TÜV SÜD experts cover the regulatory requirements for AI-based medical devices under the EU MDR and the EU AI Act,
Webinar on the implementation of the EU Medical Device Regulation and the EUDAMED database, focusing on patient safety, environmental sustainability,
Official European Commission stakeholder training webinar ahead of the EUDAMED mandatory activation on May 28, 2026. Covers the four mandatory
Legal experts from Taylor Wessing provide a deep dive into the amendments to the EU MDR and IVDR regulations, covering
Expert-led webinar on European CE marking strategies under the EU MDR, including notified body selection, technical documentation requirements, and conformity