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

    eCOA Vendor Localization Best Practices Checklist

    One of the main challenges for pharma/biotech companies regarding clinical trials is prolonged eCOA study start-up. It is paramount to choose the right eCOA platform for each study. Sponsors must consider the study’s specific needs, such as user-friendliness, compliance, and configurability. The investment of both time and money, not to mention protecting and upholding the integrity of the data collected, is critical when seeking regulatory approval and confirming ...

    eCOA Vendor Localization Best Practices Checklist

    Selecting an eCOA Vendor to Best Fit Localization Needs

    One of the main challenges for pharma/biotech companies regarding clinical trials is prolonged eCOA study start-up.  It is paramount to choose the right eCOA platform for each study. Sponsors must consider the study’s specific needs, such as user-friendliness, compliance...

    MedTech Summit EU 2024 | What's Past is Prologue: Evolution (and Future) of AI and Content Automation

    Content automation technologies have been developing for 70 years – MDR and IVDR have accelerated this development, as well as adoption across the device industry. And, while product-related applications for artificial intelligence (AI) generate attention-grabbing headlines, the ...

    Pfizer x Partner4Better Spotlight

    TransPerfect supports the development of the Global Learning Program: Partner4Better, by delivering relevant educational content to a global audience in diverse languages. ...

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

    Join TransPerfect's discussion with industry-experts from Pfizer, Bayer, CodaMetrix, Biogen, BI, Novartis, and Syneos Health about how AI is accelerating changes in the life sciences industry and ways they are leveraging data to support their teams, studies, and products. ...

    AI and MT for PV and Safety Office Hours - 6/12/24

    Welcome to TransPerfect Life Sciences' AI and MT Ask an Expert Office Hours. In these sessions, we provide an opportunity for our community to submit their pressing questions for our experts to answer live, in the company of your industry peers. If you are looking for some ...

    Strategic Artificial Intelligence (AI) Implementation for Medical Device Companies

    Medical device companies are leveraging artificial intelligence and machine learning to streamline regulated medical device content work streams, including labeling, marketing, and PMS reporting. Learn about implementing a strategic AI program and discover how top medical ...

    Rise above the complexity of clinical trials.

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