United Kingdom: Life Sciences, Biotechnology & Nanotechnology

Subscribe
Welcome to the Mondaq Food, Drugs, Healthcare, Life Sciences homepage, here you will find thought leadership articles, podcasts, videos and webinars providing insights covering topics such as Food and Drugs Law, Healthcare, Life Sciences, Biotechnology and Nanotechnology.
Article
Life Sciences Patents Monthly Roundup—September 2026
This September edition examines pivotal developments in life sciences patent law across Europe, with the Unified Patent Court continuing to refine its jurisprudence on added matter, intermediary liability, and procedural standards. National courts in the UK, France, and the Netherlands deliver significant rulings on supplementary protection certificates, pro-drugs, and the boundaries of pharmacy exemptions that will shape patent strategy for pharmaceutical and medical device companies.
European Union IP
AO
A&O Shearman
Article
Spinal Cord Injuries: Emerging Technology Update
Technology aimed at improving independence following spinal cord injury continues to develop, from mobility equipment already on the market to implantable devices that are still at an early stage of research. This article examines three different technologies and considers how developments such as these could shape the lives of people living with SCI, as well as what they might mean for future claims.
United Kingdom Healthcare
W
Weightmans
Article
Patenting Performance: Protecting The Science Behind A Personal Best
Nomio, a broccoli-based sports supplement gaining popularity among endurance athletes, has secured patent protection for its innovative use of sulforaphane to enhance exercise performance and treat metabolic conditions. This analysis explores how the company leveraged university research to protect both therapeutic and non-therapeutic applications of their simple three-ingredient formula, demonstrating that even products with common ingredients can achieve robust patent protection through novel use claims.
United Kingdom IP
HL
HGF Ltd
Article
How Low Can You Go? T 0137/24, Percentage Sequence Identity Claims And Divergent EPO And USPTO Approaches
The European Patent Office Board of Appeal's decision in T 0137/24 examines whether increasing percentage sequence identity thresholds in patent claims constitutes added matter and whether such claims meet sufficiency requirements. This case highlights the divergent approaches between European and US patent offices when evaluating biotechnology claims that define protein variants through sequence identity percentages combined with functional limitations.
United Kingdom IP
HL
HGF Ltd
Podcast
(Medical) Crimes And (Data) Misdemeanours - Writing To The European Commission’s AI Act Service Desk Concerning Annex V Of The EU AI Act (Conformity Assessments) - LIVE! (Podcast)
Marc Dautlich and Alex Denoon explore the complexities of the EU AI Act's Declaration of Conformity requirements, specifically examining what it means for High-Risk AI Systems to comply with GDPR. The podcast addresses the practical challenges providers face when preparing this living document for AI-integrated medical devices and other regulated systems.
United Kingdom Healthcare
B
Bristows
Article
Global Life Sciences & Healthcare Bulletin
Eversheds Sutherland provides legal insights and analysis through their Global Life Sciences and Healthcare Bulletin series. The firm's international team of attorneys offers guidance on regulatory developments, compliance matters, and strategic considerations affecting pharmaceutical, biotechnology, and healthcare organizations. Contact their specialized practitioners for detailed counsel on navigating complex legal frameworks in the life sciences sector.
Global Healthcare
ES
Eversheds Sutherland
Article
Aesthetics Regulation In 2026: An Increasingly Complex Regulatory Landscape
The regulation of non-surgical aesthetics in England is approaching an important turning point. Although there is not yet a comprehensive statutory licensing regime, aesthetics businesses and regulated healthcare professionals already operate within a complex framework of professional, medicines, and product regulation. Further regulation is also being developed specifically for non-surgical cosmetic procedures.
United Kingdom Healthcare
JS
JMW Solicitors LLP
Article
The EU Pharma Package: Upcoming Reform Of Regulatory Data Exclusivity And Market Protection For Approved Medicines For Human Use
The European Parliament and Council have agreed on the most significant reform of EU pharmaceutical legislation in two decades, fundamentally restructuring the regulatory data exclusivity and market protection framework for newly approved medicines. While the baseline eight-year data protection period remains unchanged, the market exclusivity system has been overhauled with a new modulated approach that reduces automatic protection and requires pharmaceutical companies to complete specific clinical studies
European Union Healthcare
PS
Penningtons Manches Cooper LLP
Article
Sustainable Fertilisers: Innovations, Patentability, And Start-Up Support In Europe
Geopolitical conflicts and climate change are threatening global food security by disrupting fertiliser supply chains and driving up costs. European companies are developing innovative solutions ranging from green ammonia production and nitrogen fixation technologies to circular fertilisers derived from waste streams and biological alternatives that enhance nutrient efficiency.
European Union IP
HL
HGF Ltd
Article
Advancing Advanced Manufacturing Capabilities In Glasgow
Glasgow's XWORKS innovation hub represents a £11 million investment in advanced manufacturing infrastructure, set to provide 45,000 sq ft of flexible workspace for mid-tech companies in clean energy, defence, space and life sciences sectors. The facility, scheduled for completion in early 2027, aims to lift technological limitations for innovators and start-ups while strengthening Glasgow's position as a destination for innovation-led businesses.
United Kingdom Real Estate
MC
Marks & Clerk
Article
Virtual And Digital Health Digest – July 2026
European regulators are accelerating AI governance frameworks while balancing innovation with patient safety in digital health. The European Commission has published voluntary codes for AI-generated content marking and appointed expert bodies to enforce the AI Act, while the UK's MHRA launches regulatory sandboxes to test AI tools in medicines development and the ICO establishes comprehensive guidance for AI-powered healthcare technologies.
United Kingdom Healthcare
AP
Arnold & Porter
See more