Reduce Friction in Your Clinical Trials to Accelerate Development Timelines

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

Streamline My Study

Featured Content Solutions That Streamline Global Development

    Comprehensive COA/eCOA Solutions

    Ensure conceptual equivalence and cultural appropriateness in any language, minimizing 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 with analysis, creation, translation, and SME support for your clinical trial and research information. Know your content 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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    Translation Services

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

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

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    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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    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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    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
    Pfizer logo
    Takeda logo
    Sanofi logo
    Johnson & Johnson logo

    Navigate Through Complex 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

    The C3 Summit: Boston Recap

    The second event in our series of C3 Summits took place in Boston on May 16, 2023. We invited industry experts and leaders to discuss challenges, opportunities, and strategies in clinical trial diversity, centricity, and outcome assessments through the lens of real-world experience. In this recap of the Boston session, we will review key points from each session.  Session 1: COA/eCOA Innovations – Licensing Hiccups, Linguistic Validation, ePRO Migration, and Best ...

    The C3 Summit: Boston Recap

    How Medical Writing Can Drive Patient Engagement

    Medical writing is a critical component of the broader patient engagement landscape, establishing the foundations of communication between pharmaceutical companies and patients. The quality of medical communication can be transformational in how a patient engages with and...

    A Conversation with Dr. Elin Haf Davies of Aparito

    The rare disease space presents numerous challenges for clinical research and patient data capture. These challenges are only heightened for younger patient populations, where outcome measures and dosages need to be considered appropriately. Join Dr. Elin Haf Davies, Founder & ...

    The C3 Summit: San Francisco Recap

    April 20 marked the first in our series of C3 Summits, which kicked off in San Francisco. Throughout the event, we invited industry experts to panel discussions to explore patient diversity, centricity, clinical technologies, and innovations. In this recap, we will briefly...

    Overcoming 5 Challenges of Implementing eClinical Technologies

    eClinical technology has transformed the clinical trial landscape, maximized data collection efficiency, and streamlined trial operations. Innovations in this space, such as electronic trial master files (eTMF), clinical trial management systems (CTMS), and electronic patient...

    Panel: Deploying AI for Translation - Real Life Examples

    Learn how leading companies deploy machine translation and the results they are seeing from their MT strategy. ...

    The Quality Review of Documents (QRD) v9.0 for Veterinarians: A Step Toward Better Care

    The Quality Review of Documents (QRD V9) update came into effect on January 28, 2022. The new version consists of a set of guidelines established by the European Medicines Agency (EMA) outlining the responsibilities and duties of those who ensure the quality of veterinary...

    Ready to launch and manage clinical trials faster?