Global Regulation & Software for Medical Devices Digital Week is a complimentary 3-day webcast series. Join us for an insightful few days as we explore regulations in APAC, EU, US and Software (MDSW) and AI/ML.

This live online training course will equip you with a working knowledge of the technical vocabulary and processes needed to make software that is both safe, secure, reliable, effective and compliant under the EU MDR. 12-13 June 2023.

Introduction to Biocompatibility LIVE Online Training Course | 2pm - 6:00pm CET

Regulatory Affairs in Latin America for Medical Devices. 12-13 March 2024

A comprehensive guide to the in vitro diagnostic industry. Take a look at the full cycle from the key players, the bigger picture, how your IVD fits into the landscape, the key regulations, and what processes you need to be aware of. Training Course.

Join us for an intensive two-day training course that provides a comprehensive update on the latest post-market surveillance and vigilance reporting requirements, emphasizing the transformative role of Artificial Intelligence. This is a 2-day training course, 8-9 October 2024. London, UK.

Medical Device School provides a comprehensive overview of the entire medical device lifecycle, through the R&D stages to the latest updates in regulatory requirements and post-market considerations. Benefit from structured learning delivered by 15 expert trainers. 5-7 Nov 24.