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

    C3 Summit 2025 - San Francisco

    Conversations on Clinical Content, C3 Summit is part of a series of events hosted by TransPerfect Life Sciences featuring sessions with expert panels discussing present challenges, strategies, and innovations, as well as insights into future advancements, from R&D to commercialization. The event offers sponsors, CROs, and biotech professionals opportunities to share knowledge, gain industry insights, and network. Please fill out the form to access the session ...

    C3 Summit 2025 - San Francisco

    Website Localization Fact Sheet

    Language barriers are a measurable enrollment risk, and one that compounds fast. With 25.7 million people in the US living with limited English proficiency and 41% of adults reporting they know nothing about clinical trials, the patient pool is larger than most teams realize and ...

    Patient Recruitment Strategies for Clinical Trials

    Most trials miss enrollment targets because patients don’t understand, trust, or act on the information they receive. The gap between a recruitment strategy built around patient comprehension and one that isn't, touches everything from screening drop-off to diversity goals. ...

    Clinical Trial Website Localization: Accelerating Enrollment and Reducing Compliance Risk

    Language barriers are a measurable enrollment risk, and one that compounds fast. The gap between a localized and non-localized clinical trial website is wider than most teams expect, touching everything from regulatory compliance to participant drop-off. This infographic breaks ...

    Medical Device Localization: Navigating Compliance and Empowering Engagement

    As medtech digital health ecosystems expand, companies face growing pressure to deliver products and information tailored to each global market. Meeting that demand requires a strategic approach to medical device translation and localization spanning cultural adaptation,...

    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 ...

    The Role of AI and Machine Learning in Clinical Outcome Assessment Translation

    Author: Mark Wade, Global Practice Leader & COA SME, TransPerfect Life SciencesThere is little doubt across the industry that artificial intelligence (AI) and machine learning (ML) have changed the game, particularly when it comes to clinical research. From using it to...