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.

    How to Select the Right Regulatory Writing Company for Your Organization's Needs

    Blog

    In a landscape defined by ever-evolving global guidelines from health authorities, many life sciences organizations’ clinical and regulatory teams face challenges in navigating the regulatory affairs writing and document submission process. Adhering to strict rules while balancing the concerns of multiple stakeholders, timelines, and costs can be a profoundly complex undertaking in this high-stakes environment. To successfully expand their products globally and ...

    How to Select the Right Regulatory Writing Company for Your Organization's Needs
    Guide

    Governing AI for Global Content in the Life Sciences Industry

    AI is already shaping the content that reaches patients, healthcare professionals, and regulators, often through tools that were never built for regulated use. But adoption alone doesn’t create control, and a single terminology error or untraceable approval can put compliance and ...
    Blog

    MDR SSCPs and IVDR SSPs Are NOT Labeling: What That Means for Your EUDAMED Upload

    As soon as possible, but no later than March 27, 2027 (per MDCG 2026-4), medical device manufacturers must upload their validated, translated Summaries of Safety and Clinical Performance (SSCPs) to EUDAMED themselves. IVD manufacturers have the same responsibility for their...
    Webinar

    Reddit Stories: AI Failures in Clinical Trials

    Clinical operations experts react to real AI failure stories pulled directly from Reddit and work backward to identify what should have caught them. From hallucinated citations that passed an initial review to AI-drafted guidance sent to a site without proper oversight, each ...
    Blog

    Are Legacy COA Instruments Still Fit for Purpose?

    The following insights are synthesized from TransPerfect LifeSci Talks, hosted by Mark P. Wade, Practice Leader COA SME at TransPerfect Life Sciences, with guest Kathrin Fischer, PhD, Patient-Centered Outcome Strategy Lead at Boehringer Ingelheim and board member of ISOQOL....
    Webinar

    The Human in the Vault: Building Review Workflows That Satisfy Regulators

    AI translation is already fast enough for most teams. The gap is on the review side: who signs off, what gets logged, and whether the process holds up when a regulator asks. This session walks through a real human review workflow within an AI-assisted translation process ...
    Blog

    eConsent: Why the Content Matters as Much as the Tech

    Insights from a conversation with Edwin Cohen, Principal Consultant / Owner at C&Flow Instrument Creation and Mark P Wade Global Practice Leader & COA SME, TransPerfect Life Sciences For all the attention paid to the systems, platforms, and integrations behind...