Overcome all of your regulatory hurdles with 8 medtech conferences and 3 workshops. Navigate EU MDR, IVDR, Software & AI, UKCA and Global Regulations, diving into the details of Clinical, Post Market Surveillance, Law and Compliance, and Biocompatibility. MedTech Summit, 16-20 June 2025, Berlin.

Keep up on trends in the transparency reporting landscape: this robust, must-attend event features essential dialogue on topics of Sunshine Act expansion, changes in state level legislation, enforcement trends, virtual HCP interactions, global transparency, risk mitigation strategies, data analytics

MedTech Event And Content Series: Industry Leading Events, Webinars, Reports And Stakeholder Perspectives To Help You Overcome Your Regulatory Challenges

MedTech Digital Week is a complimentary 2-day webcast series exploring the latest EU MDR insights, tools and guidance. 17-18 October 2023.

Explore innovations and comprehensive regulatory strategies for medical devices at our digital conference, November 5-7, 2024. Topics include ISO 13485, EU MDR, UKCA, AI/ML, RWE, 510(k)s, PCCP, Data Sufficiency and eSTARs. Insights for US, EU, and UK regulations from FDA, Notified Bodies & Industry

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.

Analyse, interpret and apply the laws regulating the provision of healthcare with particular regard to ethical perspectives

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.