US Regulation of Medical Devices
Venue: TOPRA Office, 3rd Floor City Reach, 5-6 Greenwich View Place, London E14 9NN, UK (& online)
Start: Wednesday 23 Jul 2025 09:00
End: Sunday 25 May 2025 16:30
This event is brought to you by TOPRA.
Gain a comprehensive understanding of US regulatory procedures for medical devices and develop the skills to make strategic recommendations for entering the US market. Gaining an up-to-date view on the potentially rapidly changing regulatory environment in the USA should be essential for all who aspire to participate in the world’s largest healthcare market.
By attending this training course between 23 - 25 July 2025 (in-person in London, UK or online), you will:
✅ Understand the global importance of the US medical devices market and the history and context of medical device regulation in the US.
✅ Demonstrate a critical understanding of US medical devices regulation, processes, and procedures.
✅ Evaluate the differences and similarities of the US regulations with rest of world regulatory requirements.
✅ Develop the ability to recommend a suitable strategy for entering the US market.
✅ Earn 15 CPD hours.
With an engaging programme led by Richard Vincins, Principal Strategy Consultant from North American Science Associates (NAMSA), this course is an excellent opportunity for regulatory affairs professionals and allied industries to expand their knowledge of the US medical device market.
This course is part of our range of Masterclasses and is Module 21 in our MSc programme. Our Masterclasses are developed and delivered by a faculty of expert speakers and validated by the University of Hertfordshire.
Discounted rates are available for TOPRA MSc students, those working for regulatory or government agencies, academic institutions, charities, patient groups, or in full-time education.