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  • Our Offering
    • Fractional IP counsel
    • Start-ups
    • Established pharma
    • International IP counsel
    • Investors
    • Due diligence
    • Evolve AI
    • Oppositions and appeals
  • Fractional IP counsel
  • Sectors
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    • Biologics
    • Cell & gene therapy
    • AI drug discovery
    • Chemistry
  • Evolve Insights
    • Articles
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  • About us
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    • Contact us
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  • Fractional IP counsel
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  • Evolve Insights
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Articles

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The morality (and patentability) of inventions derived by immoral means (T 2510/18)

  • 25th June 2025
Should patents be granted for inventions born from unethical practices, even if they offer significant societal benefits?

How to read a biotech patent

  • 23rd June 2025
Learn how to quickly search for and extract key information from biotech patent documents.

EBA decides G1/24 on claim interpretation: The description should always be consulted

  • 19th June 2025
Understanding how patent claims are interpreted is crucial, and a recent EPO decision, G 1/24, provides new guidance: always consult the patent’s full description and drawings, not just the claims themselves.

IP implications of the FDA guidance for use of AI in drug development

  • 17th June 2025
Learn how the FDA’s new draft guidance on the use of AI in drug development may impact the industry.

Is it time for patent offices to enter the bioinformatic age?

  • 13th June 2025
In a world in which incalculable amounts of sophisticated sequence data is freely available, are the clunky processes necessary to input patent sequence data really fit-for-purpose?

Evolve’s Steven Gurney recognised in IAM 1000 2025

  • 11th June 2025
We are delighted to announce that Evolve’s founder Steven Gurney has once again be recognised in the IAM patent 1000.

Alnylam v. Moderna and the judicious use of definitions: The European perspective

  • 10th June 2025
When drafting a patent, seemingly innocuous “boilerplate” definitions in the description can drastically narrow your claims, as demonstrated by the Alnylam v Moderna case in the US, highlighting the critical need for precise language to protect your invention.

Freedom to operate versus patentability in biotech: What the difference is and why it matters

  • 9th June 2025
Discover the critical difference between patentability and freedom to operate in biotech, and why true innovation is your best strategy for navigating the complex intellectual property landscape.

Alexion’s Soliris sequence error saga (Alexion v Samsung Bioepis [2025] EWHC 1240)

  • 4th June 2025
Beware! The recent Samsung v Alexion UK High Court decision reveals that even a single-letter error in patent sequence data, coupled with vague descriptive language, can invalidate your claims and lead to costly legal battles.

All to play for in CRISPR “first-to-invent” US patent battle as Federal Circuit instructs PTAB to reconsider (Regents v. Broad Institute, Nos. 22-1594, 22-1653)

  • 28th May 2025
Navigating the complex CRISPR patent landscape remains a challenge. The Federal Circuit’s decision in Regents v. Broad Institute is another in the ongoing battle between the inventors of CRISPR.

Event report: C5 Pharma & Biotech Patent Litigation in Europe (Day 1), Plausibility, UPC and antibody IP strategy

  • 27th May 2025
Navigating European pharma and biotech patent litigation is more complex than ever, with ongoing debates on plausibility, UPC intricacies, claim interpretation, and divergent strategies for antibody inventions.

An LLM is not (yet) a person skilled in the art (T 1193/23)

  • 20th May 2025
The EPO clarifies that an LLM interpretation of a technical term in a patent is not yet evidence of how a skilled person would interpret the term.
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