Reduce the Operational Complexity and Cost of Global Patent Translation and Filing

Protect your intellectual property with TransPerfect’s global patent filing expert. Our global coverage helps you adhere to regulatory compliance requirements around the world.

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Centralize Your Patent Management Process

As your full-service patent solutions provider, we streamline the patent filing process from start to finish. Gain peace of mind knowing your IP is protected internationally.

    Patent Translation and Filing

    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 Services

    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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    TransCEND Virtual Data Room (VDR)

    Our full-service data room platform stores internal company data and exchange translation content, so you can rest assured your content is protected against breaches.

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    Information Governance

    Protect your patents against information security threats. Our specialists will help you navigate the global regulatory landscape, monitor information compliance, manage your data, and educate your employees on corporate policies.

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    End-to-End Global Solutions for Your Most Valuable Assets

    Ensure the highest possible quality and speed for your patent translations. GlobalLink for patents helps you organize and keep track of translation and filing requests. Our powerful translation technology harnesses the power of translation memory to store and utilize translations for all future projects.

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    Pay Up to 50% Less for Translations and Attorney Fees

    Patent Translations
    • Patent Applications
    • Rule 71(3) Claims
    • Prior Art/Abstracts
    • Drawings
    • Office Actions
    • Litigation Documents
    • Sworn Translations

    Patent Filing
    • Arrange Translations
    • Instruct Filing Agents
    • Coordinate Paperwork and Payment
    • PCT National Phase Entry
    • Direct National Filing
    • EP Validation

    Patent Support by the Numbers

    60

    Jurisdictions

    2 k+

    EP Validations

    200 +

    Languages Supported

    1 k

    EP Apps

    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.

    Regulatory Considerations for Paper COA Translations | What You Need to Know

    Blog

    Collecting data for a global clinical trial on paper COAs or managing a mixed-mode study that combines both paper and electronic formats means satisfying multiple regulatory bodies before a single patient enrolls. None of these entities operate on the same timeline or answer to each other. While paper instruments might seem more flexible to deploy because they don’t require electronic implementation, there are still process considerations based on the instrument’s ...

    Regulatory Considerations for Paper COA Translations | What You Need to Know
    Webinar

    XTalks | eCOA: Has It Lived Up to the Promise? A Realistic Assessment for Today's Trials

    Despite two decades of technological advancement, the debate between paper and electronic clinical outcome assessments (eCOA) remains unresolved. This webinar revisits the assumptions that continue to shape data collection strategies and examines whether current practice reflects ...
    Webinar

    SSCPs Are Not Labeling: Compliant AI Processes for Reduced Cost & Turnaround

    In this fireside chat, TransPerfect Medical Device's President Marc Miller sits down with Dr. Keith Morel, VP of Regulatory Compliance at Qserve, to unpack a critical question facing medical device manufacturers under MDR: can you reduce the translation review process for ...
    Success Stories

    Top 10 Pharma Company Overhauls Global COA Program,Cutting Costs by 33% and Errors to Near Zero

    Inconsistent standards, stretched timelines, and limited visibility were straining a top 10 pharma company's COA program. Discover how TransPerfect Life Sciences' centralization strategy delivered 99.7% accuracy, 40% less PM oversight, and 33% cost savings across the ...
    Blog

    Four Years In: What the EU Clinical Trial Regulation Has (and Hasn't) Delivered

    When the EU Clinical Trial Regulation (EU CTR No 536/2014) went live for new submissions on January 31, 2022, it promised to transform how clinical trials are authorized and conducted across Europe: a single submission, one decision, and harmonized oversight. Four years in,...
    Webinar

    How to Make Your Academy Succeed at Global Scale—Lessons Learned on What Works and What Doesn’t

    Most life sciences and MedTech companies launch a corporate academy with strong strategic intent, whether that’s executive sponsorship, a named platform, a dedicated budget, or a curriculum mapped to business goals. After launch, however, these same organizations all too often ...
    Webinar

    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 ...

    Reduce the Cost of Global Patent Translation and Filing.

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