We recently hosted an in-person event where our experts provided a legal update shining a spotlight on the hottest issues facing the medical devices industry. We've now developed a series of webinars to provide a deeper dive on the topics covered.

Each session will offer an update on key legal issues for medical device companies in the UK, EU and US, with content aimed at practical and useful guidance to help you stay on top of the myriad of legal changes. 

Details of the series are available below. Each webinar will last 45 minutes with an opportunity for questions at the end. Please select the webinar(s) you're interested in attending when you register, and you'll receive a confirmation email with joining instructions.

Date: Tuesday 4 July @ 17:00 BST
Hosts: Alison Dennis & Nick Vollers
Distinguishing wellness products and informational products from medical devices: where is the line and how is SaMD regulated in the EU?
UK proposed approach to innovation and software devices. 
Regulation (and future regulation) of AI medical devices in the UK.

Product liability - developments in the European regime 
Date: Tuesday 11 July @ 17:00  BST
Hosts: Katie Chandler
Managing product liability risks - abnormal potential for harm, Boston Scientific, DePuy and beyond

Getting to grips with medical device regulation (EU MDR and IVDR)
Date: COMPLETED
Hosts: Alison Dennis & Nick Vollers
Understanding certificate extensions in the EU (and the UK approach) and derogation applications.
Economic operators and placing on the market.
Clinical evaluation content.
Regulatory change and effect on corporate acquisitions.

Understanding data and AI for medical devices
Date: COMPLETED
Hosts: Vicky Hordern & Thanos Rammos
EU GDPR pitfalls for medical devices.
Data privacy and clinical trials – headline European issues to be aware of and an overview of roles and lawful grounds.
The AI Act and Data Act: implications for medical devices.

Click here to register