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Medical devices

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.

Product liability & product safety

Katie Chandler recognised in The Lawyer's Hot 100 2024

29 January 2024

by Shane Gleghorn and Katie Chandler

Click here to find out more
Patents & innovation

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

19 December 2023
Briefing

by Dr. Daniel Tietjen and Katharina Hölle

Click here to find out more
Medical devices

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

27 October 2023
Briefing

by Dr. Angela Knierim

Click here to find out more
Life sciences & healthcare

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

10 October 2023
In-depth analysis

by Alison Dennis and Alice Matthews

Click here to find out more

Tools and online services

2009-000779 BANR Life sciences guides tools image

EU Medical Device Regulation guides

The implementation of the EU Medical Device Regulation (MDR) and the EU In-Vitro Diagnostic Regulation (IVDR) is fast approaching, arriving in May 2021 and May 2022 respectively. 

Our two comprehensive guides provide clarity for medical device and IVD companies who may find the sheer size and complexity of the regulations a substantial hurdle to their international expansion plans.

Request your copy

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2101-000230 BANR LIST Medical devices reg tool

MDR Medical Device Checker

Our MDR Medical Device Checker assesses the likelihood of your product falling within the scope of the Medical Devices Regulation.

Access our MDR Medical Device Checker

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