All Insights

Smart Power

Smart Power | UK renewables liability risk, investments and grid connectivity

How to guard against liability risk on projects, grid concerns and investment tactics for asset managers and developers
Life Sciences and Healthcare

Draft EU medtech revisions adjust importer and distributor roles to support supply chain resilience

Digital obligations, leaner repackaging rules and new shortage reporting tools may evolve supply chain responsibilities
Life Sciences and Healthcare

Data-driven digital health businesses challenged with balancing AI advances and tighter regulation in 2026

Hyper-personalisation, data interoperability and AI are among 2025's fast-evolving areas to continue to watch this year
Advertising and marketing regulation

Marketinglaw: January 2026

Welcome to the latest edition of Marketinglaw
Retail and Consumer

Sales in Belgium: key points to keep in mind before launching a promotional campaign

The winter sales have started, next will come the summer sales and, in between, consumers are constantly exposed to various
Intellectual property

The InterDigital and Amazon SEP saga heats up with latest Unified Patent Court judgments

UPC confirms wide anti-suit-style protection against interim-licence relief, suggesting it could extend to final relief
Life Sciences and Healthcare

Planned EU medtech changes and codified Helsinki procedure support consistent qualification and classification

EU coordination, expert panel opinions and targeted down classification are proposed to harmonise risk based outcomes
Life Sciences and Healthcare

EU drug agency to take broader coordinating role in devices and diagnostics in latest proposal

Expert panel support, shortage coordination and combined study procedures strengthen the EMA's oversight of devices
Regulatory Outlook

Advertising and marketing | UK Regulatory Outlook January 2026

Influencer marketing | AI disclosure and enforcement | Protection of children | Price transparency under the DMCCA | Subscriptions |
Life Sciences and Healthcare

EU revised device rules rebalance compliance towards simplification and proportionality

Commission proposal would streamline MDR and IVDR duties with flexible evidence, timeless certificates and tailored risk rules