Quality Solutions That Reduce Compliance Risks in Clinical Trials

Choose from specialized solutions that help you increase quality and efficiency.

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Specialized Services and Technology to Support Global Clinical Trial Operations

From e-learning and training management to quality document management technology and language services, our comprehensive solutions are designed to meet the QA needs of life sciences companies. Our experience, expertise, and technology support global product development by helping to ensure corporate and regulatory compliance.

    Training Management and Course Development

    Launch effective training and reduce training expenses. Get support with authoring training content, videos, and eLearning for compliance and streamline training delivery with LMS technology designed for global study teams and clinical sites. With Training Management, send approved and effective policy and SOPs directly to the LMS for "Read & Understand" or eSignature by staff to ensure training compliance.

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    Ensure the accuracy and consistency of global training content and simplify the rollout of multilingual training programs with industry-leading translation automation and service solutions for localization, adaptation, managed in-country review, and more. Ensure compliance with seamless "Author-to-Archive" workflows between your content repository and certified translation staff with TransPort to TI connectors.

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    QMS and Quality Documentation (Trial Interactive)

    Simplify quality management with a centralized workspace where you can create quality document templates; track them through draft, review, and approval; and then seamlessly publish to the LMS as learning modules to enforce compliance. Track and manage complaints, investigations, CAPA, audits, observations and findings, actions, effectiveness checks, and change management using standard best-practice QA workflows for GCP and GMP.

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    Achieve Greatness in the Global 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.

    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. Mitigating compliance risks by streamlining QA operations is a key strategy for preventing costly delays caused by CAPAs and inspection findings.

    7,500 +

    Studies actively managed in Trial Interactive

    100 +

    TMFs rescued mid study


    eTMF study migrations completed

    50 %

    Faster site activation

    Trusted by Life Sciences Organizations Big and Small

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


    Streamline Processes and Drive Quality to Reduce Risks.

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