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.

    IMP Labeling Workflows That Reduce Relabeling Risk and Start-Up Delays

    Investigational medicinal product (IMP) labeling sits at the heart of clinical trial supply, impacting departments across pharmaceutical organizations, from clinical operations and regulatory affairs to quality assurance and beyond. When labeling activities are managed across multiple systems, vendors and stakeholders, teams often face avoidable rework, conflicting label text versions, delayed translations, unclear approval pathways and change control gaps that can ...

    IMP Labeling Workflows That Reduce Relabeling Risk and Start-Up Delays
    Blog

    Considerations for eCOA in Global Clinical Trials

    Regulatory Considerations for eCOA Submissions in Global Clinical Trials: What You Need to KnowWhen managing eCOA in clinical trials across multiple countries, translation, linguistic validation, and electronic implementation of Clinical Outcome Assessments (COAs) are...
    Webinar

    Xtalks | EU Clinical Trial Regulation: Latest Developments and Upcoming Opportunities

    The EU clinical trial landscape has changed significantly since Regulation (EU) No 536/2014 became applicable on January 31, 2022, and sponsors now need a clear view of how the framework is operating in practice and where it may evolve next. This webinar explores the current ...
    Checklist

    Veeva RIM TMS Integration Checklist

    If your regulatory team is still downloading documents from Veeva Vault, managing translation requests by email, or tracking submissions in spreadsheets, there's a better way. Reduce complexity, close compliance gaps, and shorten your submission cycle times with this ...
    White Paper

    The Current State of AI in Translation for Clinical Content

    AI is reshaping how clinical trial content gets translated and localized, but in a regulated environment, speed can't come at the cost of accuracy or traceability. This white paper breaks down where AI delivers real value, where human oversight remains essential, and how to ...
    Guide

    The Veeva Vault RIM Translation Integration

    Managing multilingual regulatory submissions shouldn't mean chasing files across email threads and re-entering metadata by hand. This playbook breaks down how direct translation integration with Veeva Vault RIM eliminates manual bottlenecks, preserves compliance, and cuts ...
    Guide

    Buyer's Guide: Translation Management Integration with Veeva Vault RIM

    Translation bottlenecks, fragmented audit trails, and uncontrolled AI output aren't edge cases in regulatory operations; they're the predictable result of a poorly integrated workflow. This buyer's guide is built for regulatory leaders who need more than a file ...