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Amélie is a Partner in CMS’s Life Sciences & Healthcare group, specialising in legal regulatory issues affecting life sciences companies operating in the UK and in the EU. She brings over 20 years of cross-border legal experience to complex regulatory challenges.

Before joining CMS, Amélie spent a decade as senior in-house counsel at major medical device companies, giving her unique insight into clients’ practical business needs.  Her experience encompasses all aspects of the product lifecycle management, regulatory compliance strategies, crisis management, and regulatory due diligence.

With a focus on medical device regulatory affairs, digital health technologies, and horizontal regulatory frameworks, Amélie offers a distinctive combination of technical expertise and commercial pragmatism.

Insights by Amélie

COP31

COP31

06 Nov 2026 2 min read
Here to stay: Government confirms long-term recognition of CE-marked medical devices and IVDs in Great Britain

Here to stay: Government confirms long-term recognition of CE-marked medical devices and IVDs in Great Britain

23 Oct 2026 5 min read
On the Pulse Webinar Series 2026 - Autumn

On the Pulse Webinar Series 2026 - Autumn

30 Sep 2026 - 19 Nov 2026
From Pre-Market to Lifecycle: The National Commission’s 44 Recommendations on AI Regulation in Healthcare

From Pre-Market to Lifecycle: The National Commission’s 44 Recommendations on AI Regulation in Healthcare

14 Sep 2026 7 min read
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