Empowering Legal Teams with Global Solutions

Get support from legal experts helping industry-leading Life Sciences manage global legal matters at scale leveraging decades of experience, translation memory, and state-of-the art ediscovery technology.

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Digital legal

Why Legal Teams Love TransPerfect Legal Solutions

Our knowledge and experience in Legal is evidenced by our ability to create and curate strategic solutions to improve their day-to-day operations / reducing administrative burdens. 30+ years of making these solutions for you specifically, evidenced by what we do:

    Patents

    Translate your patents into one or more languages in order to file in international markets. Reduce administrative burdens and the complexity of filing patents around the world. Services include in-country filing management, translation management, and document review.

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    Litigation Support

    Manage all of your litigation support needs with TransPerfect Legal. With offices in over 100 cities worldwide and specialist teams skilled in 200 languages, protect your patents from infringement or violations around the world.

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    Translation Services

    Ensure conceptual equivalence and cultural appropriateness in any language, minimizing time-to-market, mitigating risk, and ensuring compliance in global studies.

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    Protect IP and Ensure Successful Product Commercialization

    When it comes to investigations and litigation support, TLS helps mitigate the challenges associated with e-discovery, privacy, and information security, and provides visibility into the discovery management process. Leverage our proprietary database of vetted candidates from around the world to assemble multi-language teams to support patent filings, mergers and acquisitions, product licensing, international leases and contracts, and more.

    Trusted by Life Sciences Organizations Big and Small

    Schedule a Free Consultation with Global Legal Experts.

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    News and Thought Leadership

    Industry insights from our experts. We have the experience and solutions you need to navigate life sciences complexity and bring breakthroughs from lab to launch.

    C3 Summit 2025 - London

    Conversations on Clinical Content, C3 Summit is part of a series of events hosted by TransPerfect Life Sciences featuring sessions with expert panels discussing present challenges, strategies, and innovations, as well as insights into future advancements, from R&D to commercialization. The event offers sponsors, CROs, and biotech professionals opportunities to share knowledge, gain industry insights, and network. Please fill out the form to access the session ...

    C3 Summit 2025 - London
    Blog

    From Reactive to Strategic: How AI Is Transforming Medical Information Contact Centers

    IntroductionFor decades, Medical Information (MI) has been an essential function within pharma, but largely a reactive one. This is especially true in medical information contact centers, which serve as the first line of support for HCPs and patients. When someone has a...
    Blog

    Is AI Ready to Transform COA Development?

    AI is reshaping clinical development, but its greatest value may lie not in replacing human expertise, but rather in augmenting it. Across the drug development pipeline, AI is helping teams analyze vast datasets faster, identify promising compounds earlier, and uncover...
    Blog

    Five Domains the FDA Wants You to Measure in PROs for Cancer—and Why Translation Affects All of Them

    In a recent "LifeSci Talks" episode, TransPerfect Global Practice Leader Mark Wade and Signant Health VP and eCOA Scientist Bill Byrom PhD discussed how new FDA guidance is reshaping how sponsors approach patient-reported outcomes (PROs) in cancer clinical trials. PROs...
    Webinar

    AI in Medical Information: Challenges, Opportunities, and the Path to Compliant Content at Scale

    Medical information teams are being asked to do more with less; faster turnaround, broader content demands, and zero tolerance for inaccuracy. AI offers a way forward, but adoption comes with real challenges: how do you validate accuracy, integrate literature review, and build ...
    Webinar

    Xtalks | Improve Recruitment Outcomes Through More Diverse Clinical Trials

    Since the advent of artificial intelligence (AI), medical device manufacturers have been early adopters for product enhancements. Now, manufacturers are evaluating their regulated content and other production processes for suitable applications of AI and automation technology. ...
    Blog

    Potential Impact of the EU Biotech Act Proposal on Clinical Trial Activities

    The European Commission’s proposed Biotech Act introduces changes that could reshape how clinical trials are approved and managed across the EU. While the broader package spans multiple areas of the health ecosystem, proposed updates to the EU Clinical Trial Regulation (EU...