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

    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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    Clinical Outcome Assessments

    Access end-to-end consultation, from licensing to electronic clinical outcome assessment (eCOA) migration, and improve the patient and healthcare provider experience with all types of COAs.

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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
    Pfizer logo
    Paraxel
    P&G
    Takeda logo
    Sanofi logo
    Gilead
    Vertex
    AstraZeneca
    Biogen
    BMS
    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

    Clinical Outcomes Assessments (COAs) in Clinical Trials: Copyright and Licensing

    Author: Erin Sweeney, COA Director, Linguistic Validation In clinical trials, it is usually necessary for sponsors to obtain permission to use copyrighted materials, such as clinical outcome assessments (COAs). The process to obtain these permissions is called licensing. While a seemingly complex process, it is important to understand why it is necessary, what it consists of, and what needs to be done to ensure that the sponsor is complying with all the necessary ...

    Clinical Outcomes Assessments (COAs) in Clinical Trials: Copyright and Licensing

    Localizing Platforms for Digital Health: The Importance of Post-Localization Context Review

    In a landscape defined by continuous technological advancement, many organizations in the life sciences industry strive to increase audience engagement through digital modalities, such as mobile and web applications or web portals. Building a robust technological...

    Unlocking the Power of AI and Machine Learning in Life Sciences

    Life sciences companies are putting artificial intelligence (AI) and machine learning (ML) into practice, realizing its potential to revolutionize adverse event detection, diagnostics, and more. For AI and ML to be truly effective, you need to give context to your data, teaching ...

    PRO Scheduling Considerations: Assessing Patient & Caregiver Burden in Clinical Trials

    In this episode of TransPerfect LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences sits down with Andrew Lloyd, Director at Acaster-Lloyd Consulting, to spotlight the burden of clinical research for patients, and their caregiver/family dynamics. From ...

    Achieving Global Success in Clinical Trial Recruitment

    TransPerfect's GlobalLink Connect integration with Adobe Experience Cloud enabled one of the world’s largest pharmaceutical companies to help visitors in 17 countries and 13 languages identify clinical trials that might be right for them or their loved ones. ...

    4 Immediate Applications for AI Translation in Pharma

    Precision and speed are key facets of success in the dynamic world of pharmaceutical development. To achieve these goals, AI-powered capabilities, such as machine translation (MT), can have a considerable and transformative impact.  Automated translation workstreams...

    Clinical Content Trends: 2023 Reflections and 2024 Projections

    Over the past decade, the pharmaceutical industry has transformed significantly, giving way to breakthrough therapeutics and innovations for improved patient outcomes around the world. With these changes, there’s also been significant developments in the way organizations are ...

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