Custom Solutions that Navigate Complexity in 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 Operations

From language solutions to eClinical and COA technologies, 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 improves visibility, reduces timelines, enhances quality, and mitigates risk.

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    Training & Development

    Engage your staff with tailored e-learning 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 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

    Achieve Greatness in the 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. 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 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.

    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 & ...

    Navigating the EU Clinical Trial Regulation Complexities - Current Challenges and Opportunities

    As the most significant change in the European Union clinical trial legislative ecosystem in 20 years, the European Union Clinical Trial Regulation 536/2014 (EU CTR) went live on January 31, 2022. The first-year transition period has now ended, and from January 31, 2023, EU ...

    How to Maximise Value and Avoid Failure During Life Sciences Dealmaking

    Please complete the form below to access the on-demand recording of our webinar. A fantastic expert panel of life sciences dealmaking veterans from AstraZeneca and Merck, with 100 years' collective experience, share their insights on key dealmaking strategies, best practices ...

    Centralizing Global Content Solutions for Medical Affairs

    With a rapidly evolving landscape and the introduction of new technologies and emerging therapeutics, medical affairs professionals are tasked with remaining in lockstep with the latest industry developments. From a content perspective, this means not only maintaining clear...

    Automation for MDR & IVDR: A Three-Part Seminar - Part 3: EnCompass Step by Step: A Detailed View of the Content Automation Solution to Meet MDR & IVDR Requirements

    Part 3: EnCompass Step by Step: A Detailed View of the Content Automation Solution to Meet MDR & IVDR Requirements ...

    Rise above the complexity of clinical trials.

    Let's talk about how to streamline your study. 

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