Custom Solutions that Navigate Complexity in Managing Clinical Trials

Choose from specialized solutions that help you launch and manage clinical trials more efficiently.

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Specialized Services and Technology to Support Global Clinical Trial Management

From language solutions to eClinical and COA/eCOA solutions, our comprehensive solutions are designed to meet the diverse needs of life sciences companies. Our experience, expertise, and technology support product launches across global markets and expand your clinical research worldwide, while maintaining regulatory compliance.

    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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    eClinical Solutions

    Trial Interactive’s suite of eClinical solutions, including TMF Services and TMF University and Corporate Education, improves visibility, reduces timelines, enhances quality, and mitigates risk.

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    Training & Development

    Engage your staff with tailored e-learning and training that flexes to the way they learn best. Ensure that all staff have necessary qualifications and training for the roles they serve.

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    Medical Writing

    Deliver excellent 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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    Component Content Management

    Increase content reuse by 50% with TransPerfect’s Component Content Management System (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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    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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    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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    IMP Labeling

    Scale and complete regulatory review translations for any country and any label type using our ISO-certified process. Save time and reduce risks with regulatory compliant and accurately translated IMP labels.

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    Call Center Support

    Provide a clear and comprehensive customer service support experience that offers in-language guidance and speeds up the creation and communication of critical information to patients and HCPs.

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    Regulatory Landscape in ClinOps

    Managing Clinical Trials in a Complex Regulatory Landscape

    Today, global sponsors are consistently challenged to bring products to market faster while facing evolving regulations with increased scrutiny. With the language barriers and collaboration logistics of global operations, clinical trials must be managed carefully to avoid unexpected increases in cost, time, and compliance risk. Leveraging technology can bridge these gaps and provide enhanced clinical data management. Having a global partner like TransPerfect by your side helps you focus on what matters most: saving lives.

    Artificial Intelligence in Life Sciences: Latest Developments Presented by Industry Leaders

    Improved Clinical Data Management Outcomes by the Numbers

    $ 1.2 M

    Saved by CRAs using our CTMS for day-to-day operations

    85% of clinical trials experience delays. Cutting inefficient processes and technologies is the key to increasing the likelihood of meeting your timelines.


    7,500 +

    Studies actively managed by Trial Interactive

    100 +

    TMFs rescued mid study

    3,000 +

    eTMF study migrations completed

    Trusted by Life Sciences Organizations Big and Small

    Join TransPerfect's community of over 1,000 life sciences organizations, including pharma and biotech, CROs, IRBs, and agencies.

    Rise above the complexity of clinical trials.

    Let's talk about how to streamline your study.

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    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

    Your Multilingual Trial Site SEO Success Checklist

    Multilingual trial SEO is critical to ensure that patients and HCPs can actually find and act on your trial content in their language. This checklist walks clinical trial teams through five essentials:… ...

    Why Global Medical Affairs Can’t Ignore Website Localization

    A hospital pharmacist in Spain noticed a potential adverse event trend and looks for official guidance on the pharmaceutical product’s website. The safety reporting page exists, but only in English, and with dense regulatory language that’s hard to interpret quickly. The...

    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 ...

    How Medical Communications Teams Can Scale Reviews Without Sacrificing Speed

    Medical communications teams are under mounting pressure to review more content than ever before without adding headcount or increasing risk. This white paper outlines five pillars for rethinking MLR workflows, from modular content and tiered reviews to automation and governance. ...