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.

    News and Thought Leadership

    The Imperative of Accurate Translations in Clinical Research

    With the increase of global clinical trials, clinical documentation is required to be accurately translated at every stage from lab to launch. Despite the administrative burdens and tight regulatory timelines that clinical teams face, accuracy cannot be sacrificed in life science translations. Not only does accurate translation help clinical research teams overcome language and cultural barriers for global reach, but it’s also essential to mitigate ethical concerns, ...

    The Imperative of Accurate Translations in Clinical Research

    How to Improve the Speed and Accuracy of Patient Communications in Clinical Development

    According to Phesi, more than a quarter of clinical trials conducted in 2023 were canceled during Phase II.  As clinical research teams struggle with patient recruitment and engagement under tight deadlines and immense regulatory pressure, patients also grapple with...

    Implications of AI in Healthcare and Life Sciences: Ethical Considerations in the Age of AI

    Artificial intelligence (AI) models have already shown transformative potential in the life sciences industry, including automating administrative clinical research tasks, analyzing patient data to predict future health risks, synthesizing medical information, and more. ...

    The Ultimate Guide to AI in Pharmacovigilance and Safety Reporting

    Pharmaceutical companies face stringent compliance requirements and tight deadlines for reporting safety cases throughout clinical research and development. To protect patient safety and avoid penalties from regulatory authorities, pharmacovigilance teams must submit in-language ...

    E-Learning in Pharma: Creating & Managing Global Training Programs

    From compliance and standard operating procedures (SOPs), to product info and sales techniques, e-learning ensures global teams have access to top-notch, consistent, and on-demand training. This guide explores key considerations for effective and engaging global e-learning ...

    Pragmatic Use Cases for AI in Pharmacovigilance and Safety

    The rapid rise of artificial intelligence presents an opportunity for effective and transformative applications in pharmacovigilance. Intake, query routing and response, case reporting, HAQs, and more are now extremely feasible use cases that create exponential efficiency in ...

    3 Ways to Leverage Generative AI in Pharmacovigilance

    Despite the rigorous drug safety and efficacy standards in trials, study medicines can have unintended side effects on patients throughout the clinical trial journey and even in the post-market setting. To ensure patient safety and mitigate risk, global health regulatory...

    Rise above the complexity of clinical trials.

    Let's talk about how to streamline your study. 

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