A Faster Way to Complete Global Regulatory Submissions

Choose consulting and content solutions that help you clear regulatory hurdles and demonstrate product safety and effectiveness.

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Solutions That Expedite Regulatory Submissions

Content translation for regulatory submissions can shift deadlines, slow cycle times, and delay product releases. Find solutions for expediting submissions in a safe, timely, and cost-effective way.

    Product Information Translations

    Mitigate risk of human error in label production with labeling management technology that creates savings of up to 40% in translation and project management costs of global submissions (including centralized procedures in Europe, dossiers in Latin America or Asia, and Health Canada submissions).

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    Medical Writing

    Deliver first-class medical writing with analysis, creation, translation, and SME support for your regulatory documentation. Know your content is clear, concise, and follows global regulations.

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    Regulatory Translation Management

    Manage the translation of regulatory documents within one AI-powered ecosystem, integrated with Veeva and other RIMs, to ensure compliance and facilitate market access and approval.

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    eCTD Support

    Seamlessly integrate translated regulatory documents into electronic Common Technical Document (eCTD) format for efficient submission and review.

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    Navigate the Complexity of Global Regulatory Submissions

    TransPerfect helps regulatory departments reduce filing timelines and avoid critical errors and regulatory roadblocks. TransPerfect's word and phrase database generates savings by eliminating duplicate translations, which shortens overall timelines. With offices in over 100 cities and a worldwide network of experts specifically trained in mitigating risks associated with terminology and template non-compliance, there is no better partner to support your regulatory and labeling requirements than TransPerfect Life Sciences.

    Streamlined Regulatory Submissions by the Numbers

    40 %

    Savings in translation and project management costs

    140 +

    Offices in major cities

    125 k

    Global clinical studies supported

    30 +

    Years of experience

    Ready to mitigate the obstacles from global regulatory submissions?

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    Regulatory Translation Solution Saves $1.1M for Global Pharma Company

    regulatory writing

    TransPerfect Life Sciences centralizes and integrates regulatory affairs global translations with GlobalLink and Veeva RIM.

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    News and Thought Leadership

    Our industry experts have in-depth understanding of the challenges, requirements, and goals for life sciences organizations.

    Integrating eCOAs and Digital Health Technologies for Patient-Centric Trials

    The foundation of patient-first design is technology that connects seamlessly to support and meet patients where they are. In this session, leaders from Pfizer, THREAD, Datacubed, Obvio Health, and Merative will discuss how integrated digital ecosystems are breaking down platform and industry silos, enhancing engagement, improving access, and scaling across therapeutic areas. Learn how pharma and tech companies are expanding digital endpoints and paving the way for ...

    Integrating eCOAs and Digital Health Technologies for Patient-Centric Trials
    Webinar

    GenAI Strategies for Life Sciences: Creating Content that Performs, Complies, and Resonates

    Everyone’s talking about GenAI, but what does it really mean for pharma communications and promotional materials? Join our life sciences and AI experts in a follow up session from Search, Reinvented Evolving SEO in the Era of LLMs and GenAI, where we’ll take a closer look ...
    Webinar

    Transforming Medical Affairs Practices with AI and Automation for Scalable Impact

    Life sciences organizations are turning to AI to enhance operational efficiency, and one of the hottest areas of interest is the integration of AI and automation for medical affairs workflows. Beyond process optimization, automation has been accelerating omnichannel strategies by ...
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    C3 Summit - 2025 | San Francisco

    | AC Hotel San Francisco Airport/Oyster Point 1333 Veterans Blvd, South San Francisco, CA 94080 ...
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    Structured Content Simplified: A Practical Guide for Veeva, XML, and Beyond

    Life sciences organizations are facing increasing pressure to deliver accurate, compliant content across multiple channels and global markets faster than ever. To keep pace, many are turning to Structured or Component Content Management Systems (SCMS/CCMS), which allow teams to ...
    Blog

    AI-Powered Literature Monitoring for Medical Affairs & Medical Information Teams

    Written by: Gigi Shafai, Pharm.D., Vice President, Medical Affairs & Digital Transformation, TransPerfect Life SciencesStreamline your global literature monitoring activities and facilitate your Medical Affairs workflows and content development with AI-Powered literature...
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    Improving Learning Outcomes in Life Sciences Through Data-Driven Benchmarking

    Whether onboarding new commercial staff, refreshing regulatory requirements, or preparing clinical teams for new protocols, the goal of training remains the same: equip people with the knowledge and skills they need to succeed. During our recent webinar, Jessica Peyser,...