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 Ultimate Clinical Trial Translations Checklist

    Clinical product development is an elaborate endeavor executed through a complex web of processes that are in large part accomplished through various document and communication work streams. These work streams can represent a significant source of cost, risk, and time. When a study operates across cultures, countries, and continents, these pain points of cost, risk, and time are compounded by the addition of translation and localization requirements. Study teams ...

    The Ultimate Clinical Trial Translations Checklist

    CCMS: A Good Fit for Pharmaceutical and Clinical Research Organizations?

    Kaarin Gordon discusses the choices and challenges for efficient content reuse facing Pharmaceutical and Clinical Research Organizations. What they want is a set of tools and platforms for easy content reuse, automatic propagation of changes from a single source, and content ...

    Omnichannel Marketing for the Pharmaceutical Industry

    With rapid globalization and expanded marketing efforts, pharmaceutical organizations are discovering that pivoting from multichannel marketing to omnichannel marketing is key to revolutionizing patient engagement. Through tailored experiences across relevant channels, your teams ...

    LifeSci Talks COA Series | The Future of Capturing Patient Data in Clinical Trials: DCTs, Site Staff Burden, and Regulation Considerations with Paul O'Donohoe

    Mark Wade interviews Paul O'Donohoe, Senior Director of Product for eCOA and COA at Medidata. They delve into the challenges and opportunities of adopting decentralized clinical trials (DCTs) and explore topics such as mixed modalities for data capture, patient burden, site ...

    Walking the Tightrope: Navigating Patient Centricity and Burden in Modern Clinical Trials

    Over the past few decades, clinical trials have witnessed remarkable developments - but they are not without challenges. Dropout rates of up to 20% indicate that patient burden and engagement remain key areas of concern. In response to this, sponsors, healthcare providers,...

    Health Canada's XML Mandate: Pioneering the Future of Pharmaceutical Content

    In 2019, Health Canada initiated a significant process to transition all product monograph templates into a more advanced and structured XML format. This move by the regulatory authority has raised several questions for Canadian pharmaceutical organizations' regulatory and...

    Leveraging Technology and Bridging Gaps for Enhanced Clinical Data Management

    Introduction: In the field of clinical research, a robust data management process is essential for driving success. Efficiently handling vast amounts of data, ensuring accuracy and consistency, and extracting meaningful insights are vital, particularly in the case of global...

    Reduce the Cost of Global Patent Translation and Filing.

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