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The justified unequal treatment of economic operators from third countries

by Anne-Sophie van Beek

The primary subject matter of the contract is decisive in determining whether a procurement procedure must be followed

by Stef Geelen

The often-overlooked requirement to specify the maximum value

by Bram Nijhof

Online coaching and distance learning: Federal Court of Justice clarifies application of the Distance Learning Protection Act

by multiple authors

Announcing 26 senior promotions for 2026 including four new partners

by Shane Gleghorn

Vendor lock-in is no carte blanche for a direct award

by Emma Kranendonk

All change for the UK's product safety regime?

by Katie Chandler and Matthew Caskie

Use of Open-Source Software in Critical Infrastructures: Legal Framework and Requirements in Corporate Practice

by David Mallmann, LL.M. (Berkeley) and Dr. Carsten Schulz

The duty to ensure AI literacy

by Jan Rataj

China’s 2025 Trademark Law (Draft Revision): Key Amendments & Practical Impacts

by Min Dai

Proposed Amendments to the EU Medical Device Regulation

A European Perspective #1 | The Commission’s proposed MDR/IVDR reform introduces substantial changes to certification, classification and compliance frameworks. Medical device companies should assess potential im-pacts early and prepare for a shifting regulatory landscape.

by Bartosz Świdrak

2 of 9 Insights

Impact of the new Biotech Act on Clinical Trials in the EU

A European Perspective #1 | EU Biotech Act: Faster Clinical Trial Approvals Ahead | The European Commission’s proposed Biotech Act aims to streamline clinical trial procedures, shorten approval timelines, and harmonise data protection rules across the EU. If adopted, the reform could significantly accelerate multinational clinical research in the EU.

by Irina Rebin

4 of 9 Insights