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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.

Sciences de la vie et Santé

Transitional periods, extensions and derogations – help for manufacturers waiting for their MDR certificates

12 décembre 2022

par Alison Dennis

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Sciences de la vie et Santé

Proposal for an extension of transition times for the EU MDR

8 décembre 2022

par Alison Dennis

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Sciences de la vie et Santé

Has the MDCG found the answer to the slow rate of MDR certifications?

1 novembre 2022

par Alison Dennis

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Sciences de la vie et Santé

Possibilities of special permissions for medical devices on national markets

12 septembre 2022
Briefing

par Dr. Daniel Tietjen

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