Reduce Friction in Your Clinical Research to Accelerate Development Timelines

Choose industry-leading clinical research solutions to gain efficiency where you need it most.

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Featured Content Solutions That Streamline Global Clinical Research and Development

    Comprehensive COA/eCOA Solutions

    Ensure conceptual equivalence and cultural appropriateness in any language with comprehensive COA/eCOA solutions. Minimize time-to-market, mitigating risk, and ensuring regulatory compliance in global studies.

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    Medical Writing & Publication Services

    Deliver first-class medical writing in clinical research with analysis, creation, translation, and SME support for your clinical trial and research information. Know your clinical research writing is clear, concise, and follows global regulations.

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    AI Data Solutions

    Streamline the translation management process from submission to review by deploying artificial intelligence technologies, a comprehensive tracking system, and easy-to-use functions—all on an entirely secure server.

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    Content Reuse

    Increase content reuse by 50% with TransPerfect’s CCMS. Reuse content, propagate changes, enable omnichannel delivery, and streamline the review and approval process to reduce cycle time and costs.

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    Clinical Research Translation Services

    Meet multilingual challenges of document translation with powerful technology and expert linguist support to alleviate manual project management burdens associated with the clinical research translation process.

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    eClinical

    Expedite timelines, reduce compliance risks, and improve operational excellence with TransPerfect’s eClinical solution. Trial Interactive’s 21 CFR part 11-compliant unified eClinical platform provides solutions from site identification to eTMF archive.

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    GlobalLink

    Simplify the entire process from submission to release with GlobalLink translation management technology. Improve translation quality, expedite timelines, decrease workloads, and see significant cost savings.

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    Medical Device Solutions

    TransPerfect Medical Device Solutions is the first supplier to combine ISO 13485-, 14971-, and 9001-certified, patented language services with validated process automation technologies to meet the content management challenges of evolving regulations.

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    Clinical Research Solutions That Reduce Risk and Cost and Increase Quality and Efficiency

    Clinical Trial Management

    Simplify clinical content management and oversight, reduce operational costs by up to 40%, and accelerate therapeutic breakthroughs with our eClinical platform.

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    Pharmacovigilance and Safety Solutions

    Observe, detect, and monitor the effects of your pharmaceutical products across locations and languages with translation and call services. Ensure drug safety across your entire portfolio.

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    Quality

    Improve compliance and reduce risk with our Trial Interactive quality management system and study team training that ensure patient safety and remove the barriers that delay product launches.

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    Patient Services

    Deploy evidence-based patient engagement tools to increase compliance and elevate product readiness. Meet the ever-growing needs of patient-centric and inclusive solutions.

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    Clinical Trial Disclosure

    We offer a full suite of clinical trial disclosure services led by transparency subject matter experts to meet requirements and publish clinical trial results with speed and quality in any language.

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    Trusted by Life Sciences Organizations Big and Small

    Boehringer Ingelheim
    Moderna
    Novartis
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    Paraxel
    P&G
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    Gilead
    Vertex
    AstraZeneca
    Biogen
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    Johnson & Johnson logo
    Merck

    Navigate Through Complex Clinical Research Translation Processes With Confidence

    85% of studies experience significant delays. Streamline your operations and be the 15%. Join the 125,000+ studies across 110 countries supported by our industry-leading content solutions.

    40 %

    Reduction in R&D costs


    50 %

    Reduction in submission time

    35 %

    Reduction in patient enrollment time

    70 %

    Reduction in compliance risk

    News and Thought Leadership

    Scaling Clinical and Regulatory Content with GlobalLink's Intelligent Performance

    A Top 10 pharma needed to accelerate clinical and regulatory translations without increasing compliance risk or slowing submissions. This case study shows how they kept content inside Veeva Vault with an automated integration and a hybrid model (AI + validated translation memory + expert review), delivering millions in savings and getting hundreds of working days back while improving quality oversight across… ...

    Scaling Clinical and Regulatory Content with GlobalLink's Intelligent Performance

    Clinical Trials Translation Management: A Scalable Workflow for Faster Enrollment

    When it comes to clinical trials, website localization isn’t just about translating words into other languages. It’s about designing a governed, repeatable workflow that keeps every multilingual page accurate, reviewable, and in sync as content changes. This ensures patients,...

    7 Workflow Hacks for Smarter Clinical Trial Localization

    Imagine this: a director of clinical operations at a mid-size pharma needs better regional recruitment to hit aggressive enrollment deadlines. So, they push to launch the company website in nine languages at once. The moment the request lands, the clinical compliance manager...

    LifeSci Talks COA Series | Building Fit-for-Purpose PRO Instruments: Focused Modern Measures Over General Instruments

    In this episode of LifeSci Talks, Mark Wade, Global Practice Leader & COA SME at TransPerfect Life Sciences, is joined by Katja Rudell, VP of Patient-Centered Outcomes at Kielo Research, to take a behind-the-scenes look at the reality of patient-centered instrument ...

    Web Localization Playbook for Clinical Trials

    Clinical trial websites are recruitment engines. Every update must stay accurate, compliant, and consistent across languages. Yet many teams still manage localization with file handoffs, dev tickets, and manual copy/paste that can’t scale. This playbook covers… ...

    Back to the Basics: Foundations of COA Localization

    This blog is a follow-up from our webinar Foundations of Clinical Outcome Assessment Localization.Clinical outcome assessments (COAs) play an increasingly central role in capturing how patients feel, function, and experience their condition or treatment. Yet as studies...

    LifeSci Talks COA Series | Meaningful Patient Involvement in HTA Decision-making: Where do we go from here?

    In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with Alice Biggane, Outcomes Innovation and Research Lead at Pfizer, to discuss how PRO measures inform and impact endpoint adjudication and reimbursement decisions, due ...

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