Course: Regulating Medical Devices – 24th April

Thursday 24th April 2025: 13:00 – 14:30 via Zoom

Free for NHS staff if booked with their nnuh.nhs.uk email address

Navigate the Path to Regulatory Approval for MedTech!

Understanding regulatory approval is key to bringing your medical technology to market as without demonstrating compliance with regulatory standards, you will not get market authorisation. This course will guide you through the process of obtaining UKCA and CE marks, as well as the FDA approval process, while addressing key regulatory questions and documentation requirements.

Learn from expert Chris Warwick how to develop a strategic plan to meet compliance standards across the UK, EU, and international markets.

To book your place, click here.