Industry News
The latest medical device regulatory news, clinical trials, and market insights
FDA Webinar: eCTD 4.0 Migration for Medical Device Submissions
Training on the transition to eCTD 4.0 electronic submission standard for medical device regulatory filings with the FDA. Register /…
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.…
Greenlight Guru Webinar: Design Controls for Medical Devices – Practical Guide
Free webinar covering practical design control processes for medical device development, including design inputs, outputs, verification, and validation under FDA…
MedTech Europe Webinar: EUDAMED Onboarding – UDI Registration Practical Guide
MedTech Europe webinar combining regulatory context with practical operational guidance for EUDAMED UDI registration ahead of the May 28, 2026…
BSI Webinar: What Class C IVD Device Manufacturers Must Do Now Under IVDR
BSI notified body experts discuss the regulatory requirements and transition timelines for Class C IVD device manufacturers under the EU…
Qserve Group Webinar: EU MDR 2.0 Revision – What Changes Are Coming
Qserve regulatory experts analyze the proposed EU MDR and IVDR revision (MDR 2.0), covering changes to software classification, AI Act…
TÜV SÜD Webinar: Artificial Intelligence (AI) in Medical Devices – Regulatory Requirements
TÜV SÜD experts cover the regulatory requirements for AI-based medical devices under the EU MDR and the EU AI Act,…
Health Care Without Harm Europe: Safer Medical Devices – EU MDR and EUDAMED Implementation
Webinar on the implementation of the EU Medical Device Regulation and the EUDAMED database, focusing on patient safety, environmental sustainability,…
European Commission: EUDAMED Mandatory Modules – Stakeholder Training Webinar
Official European Commission stakeholder training webinar ahead of the EUDAMED mandatory activation on May 28, 2026. Covers the four mandatory…
Taylor Wessing Webinar: EU MDR/IVDR Amendments – Legal Deep Dive
Legal experts from Taylor Wessing provide a deep dive into the amendments to the EU MDR and IVDR regulations, covering…
Emergo by UL Webinar: European CE Marking Strategy for Medical Devices 2026
Expert-led webinar on European CE marking strategies under the EU MDR, including notified body selection, technical documentation requirements, and conformity…
BSI Webinar: MDR General Safety and Performance Requirements – Practical Guidance
BSI notified body webinar covering the general safety and performance requirements (GSPR) under the EU Medical Device Regulation, with practical…