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Dispositifs médicaux

Our specialist medical device team work with diverse global companies within the industry to sustain growth, exploit current and future innovations, and secure their business's success. Our clients are multinational corporations and start-ups within the medical devices industry from companies within medical devices or in vitro diagnostic medical devices.

With sector-specific expertise grounded in scientific intelligence and technological know-how, clients value our knowledge of the regulatory frameworks shaping clients' strategic options, the technology being deployed, and our ability to execute complex legal solutions across multi-jurisdictions.
We ensure that our clients operate within the boundaries of medical regulations, data privacy, competition/anti-trust, procurement, pricing and reimbursement, advertising and promotion, and anti-bribery compliance/fraud and abuse laws.

We are pivotal in leveraging growth through strategic alliances, fundraisings, IP and compliant data privacy and security activities, and are relied on to resolve both offensive and defensive cross-jurisdiction patent litigation.

With in-depth sector expertise, we also actively engage with the wider medical devices industry through our connections with esteemed industry bodies and as leading voices in industry publications and wider expert webinar/seminar series.

Responsabilité du fait des produits et de la sécurité des produits

Katie Chandler recognised in The Lawyer's Hot 100 2024

29 janvier 2024

par Shane Gleghorn et Katie Chandler

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Brevets et innovation

Higher Administrative Court of Münster: Subsequent authorization of a homeopathic medicinal product

19 décembre 2023

par Dr. Daniel Tietjen et Katharina Hölle

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Dispositifs médicaux

Artificial Intelligence (AI) in medical devices: The better the product, the harder the conformity assessment?

27 octobre 2023

par Dr. Angela Knierim

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Sciences de la vie et Santé

Updated post-market surveillance (PMS) rules for medical devices in the UK: differences from the EU regulations

10 octobre 2023
In-depth analysis

par Alison Dennis et Alice Matthews

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