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.

Learn More
global

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).

    Learn More

    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.

    Learn More

    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.

    Learn More

    eCTD Support

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

    Learn More

    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?

    Get in touch ›

    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.

    CAPTCHA
    This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
    Webinar cover image
    CAPTCHA
    This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.

    News and Thought Leadership

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

    Localizing Health Apps at Global Scale: UI/UX Considerations

    Blog

    With 200 new mHealth (mobile health) apps launching daily, it’s safe to say that the digital health market is exploding. For health-tech startups and established organizations looking to scale across global markets, the differentiator in a competitive landscape isn’t always the features—it’s the user experience. Recently, TransPerfect Life Sciences’ digital health experts hosted a webinar breaking down how organizations can build global-ready mobile apps. Below are ...

    Localizing Health Apps at Global Scale: UI/UX Considerations
    Webinar

    Integrating AI to Scale & Accelerate Workflows and Improve Pharma Product Launches

    Bringing a new medical product to market has always been a challenge, though advances in recent tools have promised a new age of streamlined processes and accelerated time to launch. However, most pharma commercial AI pilots never make it past proof of concept due to siloed ...
    Webinar

    Optimizing COA/eCOA Workflows with Technology for Better Quality & Timelines

    Efficient workflows are critical to keeping global COA/eCOA studies on schedule while ensuring the quality of localized content. This live webinar will explore how technology stacks and automation can streamline clinical localization from start to finish, through integrating ...
    Webinar

    Global by Design: Localizing UI/UX for Health Mobile Apps

    In today’s global digital health landscape, localization goes far beyond translation. In health mobile applications, it means tailoring the user experience to cultural, linguistic, and even regulatory nuances across different regions. This discussion explores how localization in ...
    Blog

    Immediate Use Cases for GenAI in Pharma

    AI’s promise for the life sciences industry is enormous. Equally enormous is the hesitation to leverage it. Many organizations never make it past the pilot (if that), convinced they must solve every data challenge or build complex, validated AI pipelines from the get-go.In...
    Blog

    From Documents to Data: A New Paradigm for Pharma in the Age of AI

    Artificial intelligence has become the buzzword of the decade in life sciences. From discovery to development to regulatory submission, every function is exploring how to embed generative AI into its processes. Yet for most pharmaceutical organizations, a sobering truth...
    Blog

    Integrating eCOAs and Digital Health for Patient-Centric Trials

    A New Era of Patient-First Design Clinical research is undergoing a fundamental transformation as technology takes on a larger role in how trials are designed and executed. This shift is not simply about digitizing paper-based processes, but about creating ecosystems...