(Bio)Pharmaceuticals

In the fast-moving world of (bio)pharmaceuticals, innovation is everything. Protecting your intellectual property, navigating complex regulations and structuring the right commercial agreements are critical to attracting investment, enabling growth and bringing life-changing therapies to market. Early, strategic legal advice can make the difference between a successful venture that advances a new drug to clinical trials and on to market and a missed opportunity.

Legal advice for (bio)pharmaceutical start-ups and scale-ups

Combining intellectual property, commercial, regulatory and legal advice, our team helps (bio)pharmaceutical innovators maximize business value and investment potential. Stratiphy offers one cohesive team, tailored to your company’s needs, delivering joined-up thinking across every stage of your journey

What our clients say

“Mark Lubbock is a high-level operator and tremendously impressive in negotiations.”

— Chambers UK 2021

Services

We offer joined-up thinking across a comprehensive range of services:

IP strategy development and optimization

Proactive advice on patents and exclusivity

Leveraging IP and exit strategies

Commercial agreements

Competitor monitoring and litigation support

Legal Layer®: guiding you to the best outcome

Our team's fully-connected approach can help you to understand how your dealings with data and algorithms engage different aspects of IP and related areas of law.  In this way, we serve as a “Legal Layer” to help you optimize outcomes for your business.

Speak to an expert

Our innovative combination of experienced specialists

Our advisors bring together a wealth of experience in IP strategy and commercial law. We understand the importance of IP in both protecting future revenue streams and, in the nearer term, optimising your investment and collaboration potential. With deep sector knowledge and a practical approach, we help you navigate the complexities of the (bio)pharmaceutical landscape with confidence.

Gareth Probert
Partner, UK and European Patent Attorney, UPC Representative
Monika Rai
Partner, UK and European Patent Attorney, Solicitor, UPC Representative
Tim Belcher
Partner, UK and European Patent Attorney, UPC Representative

Discover our featured insights

Stay informed with the latest Consulting developments and the global IP landscape. Tune into our EIP Talks podcast, explore expert insights and browse our published articles and thought leadership, all designed to keep you ahead in the world of intellectual property.

Provisional Agreement Reached on the EU Pharma Package: Takeaways for Pharmaceutical Companies
February 17, 2026
The EU’s new Pharma Package will overhaul regulatory exclusivity, orphan drug incentives, antimicrobial innovation, and generic entry pathways, reducing standard protection periods while introducing new rewards like transferable exclusivity vouchers.
What should you look to protect in a (bio)pharma IP strategy?
November 18, 2025
Potential investors and development partners will expect to see an IP portfolio and strategy which maximises protection for the assets under development.
Biopharma Strategy in 2026: Lessons from 2025 on AI, M&A and the UPC
April 13, 2026
This article looks back on a selection of key trends in the (bio)pharma industry in 2025 and looks ahead to how these may continue to develop into 2026.
Why competitor patent monitoring is critical to your drug development strategy
April 15, 2026
This article explains why competitor IP monitoring is a critical part of an effective drug development strategy. By tracking competitor patent activity, companies can assess freedom to operate, identify risks and opportunities early, and make informed decisions on patent filings, licensing, and investment readiness. Ongoing monitoring also supports FTO analysis, third‑party observations, oppositions, and litigation strategy, helping life sciences businesses protect value and reduce risk throughout development.
Antibody Patent Protection in Europe and the US: Navigating EPO and USPTO Differences
April 16, 2026
This article explores the complexities of patenting antibody therapies, focusing on the differing requirements and practices of the European Patent Office (EPO) and the United States Patent and Trademark Office (USPTO). It highlights how the scope of claims, inventiveness standards, and supporting data requirements vary between jurisdictions, and explains why a tailored IP strategy is essential for innovators especially SMEs seeking protection in both Europe and the US. The article also outlines how EIP’s transatlantic teams collaborate to optimise patent applications for success in these key markets.
A truly global team

Find the right match for you

We work closely with clients, from C-suite to IP teams, to unlock the full potential of their intellectual property. Our integrated team of litigators, patent attorneys and commercial IP experts helps drive business growth by protecting and strategically leveraging patents.

Search by expertise, industry or location to find the right team for your business.

Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.