
16 June 2026Publication
CJEU clarifies MDR distributor due diligence
On 4 June 2026, the Court of Justice of the European Union (CJEU) issued its judgment in Case C 10/24 Dürr Dental SE v Cattani Deutschland Helmes GmbH & Co. KG
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Advising 3M UK in its defence of a multi-million dollar Commercial Court claim brought by Porton Capital Technology Funds and others (and their subsequent appeal to the Court of Appeal) This was in relation to allegations of breach of contract arising out of the cessation of the commercialisation of a product developed for the clinical detection of MRSA.
Advising the director of a UK-based pharmaceutical company, in his defence in the High Court and on appeal to the Court of Appeal, against claims of fraudulent and negligent misrepresentation and misstatement. This was in relation to an investment made in the company during its attempted commercialisation in the EU of a protein reverse-engineered from HIV and used for multiple therapeutic applications including treatment of ulcerative diseases of the gut.
Acting for the management of a Dutch biomedical company in inquiry proceedings before the specialised Enterprise Division of the Amsterdam Court of Appeal concerning issues of alleged corporate mismanagement in a hostile take-over context.
If you have any questions, contact a member of the Healthcare and Life Sciences Disputes team for assistance:

16 June 2026Publication
On 4 June 2026, the Court of Justice of the European Union (CJEU) issued its judgment in Case C 10/24 Dürr Dental SE v Cattani Deutschland Helmes GmbH & Co. KG

11 March 2026 Publication
The EC proposes reforms to simplify MDR/IVDR, ease burdens, boost innovation, and address device shortages, with adoption expected by summer 2026

10 February 2026 Publication
New EU Guidelines for human medicines variations apply from 15.01.2026, requiring risk-based, proactive change management and stricter documentation by MAHs.
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08 January 2026 Publication
The EC has published a proposal that may result in (IV)MD no longer being subject to AIA HRAIS requirements.

12 December 2025 Publication
EU agrees on major pharma reform, enhancing innovation, access, and protection—biggest update to pharmaceutical rules in over 20 years.