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. 

    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



    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.

    The C3 Summit: Boston Recap

    The second event in our series of C3 Summits took place in Boston on May 16, 2023. We invited industry experts and leaders to discuss challenges, opportunities, and strategies in clinical trial diversity, centricity, and outcome assessments through the lens of real-world experience. In this recap of the Boston session, we will review key points from each session.  Session 1: COA/eCOA Innovations – Licensing Hiccups, Linguistic Validation, ePRO Migration, and Best ...

    The C3 Summit: Boston Recap

    How Medical Writing Can Drive Patient Engagement

    Medical writing is a critical component of the broader patient engagement landscape, establishing the foundations of communication between pharmaceutical companies and patients. The quality of medical communication can be transformational in how a patient engages with and...

    A Conversation with Dr. Elin Haf Davies of Aparito

    The rare disease space presents numerous challenges for clinical research and patient data capture. These challenges are only heightened for younger patient populations, where outcome measures and dosages need to be considered appropriately. Join Dr. Elin Haf Davies, Founder & ...

    Navigating the EU Clinical Trial Regulation Complexities - Current Challenges and Opportunities

    As the most significant change in the European Union clinical trial legislative ecosystem in 20 years, the European Union Clinical Trial Regulation 536/2014 (EU CTR) went live on January 31, 2022. The first-year transition period has now ended, and from January 31, 2023, EU ...

    How to Maximise Value and Avoid Failure During Life Sciences Dealmaking

    Please complete the form below to access the on-demand recording of our webinar. A fantastic expert panel of life sciences dealmaking veterans from AstraZeneca and Merck, with 100 years' collective experience, share their insights on key dealmaking strategies, best practices ...

    Centralizing Global Content Solutions for Medical Affairs

    With a rapidly evolving landscape and the introduction of new technologies and emerging therapeutics, medical affairs professionals are tasked with remaining in lockstep with the latest industry developments. From a content perspective, this means not only maintaining clear...

    Automation for MDR & IVDR: A Three-Part Seminar - Part 3: EnCompass Step by Step: A Detailed View of the Content Automation Solution to Meet MDR & IVDR Requirements

    Part 3: EnCompass Step by Step: A Detailed View of the Content Automation Solution to Meet MDR & IVDR Requirements ...

    Reduce the Cost of Global Patent Translation and Filing.

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