Reduce Friction in Your Clinical Research to Accelerate Development Timelines

Choose industry-leading clinical research solutions to gain efficiency where you need it most.

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Featured Content Solutions That Streamline Global Clinical Research and Development

    Comprehensive COA/eCOA Solutions

    Ensure conceptual equivalence and cultural appropriateness in any language with comprehensive COA/eCOA solutions. Minimize time-to-market, mitigating risk, and ensuring regulatory compliance in global studies.

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    Medical Writing & Publication Services

    Deliver first-class medical writing in clinical research with analysis, creation, translation, and SME support for your clinical trial and research information. Know your clinical research writing is clear, concise, and follows global regulations.

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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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    Content Reuse

    Increase content reuse by 50% with TransPerfect’s 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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    Clinical Research Translation Services

    Meet multilingual challenges of document translation with powerful technology and expert linguist support to alleviate manual project management burdens associated with the clinical research translation process.

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    eClinical

    Expedite timelines, reduce compliance risks, and improve operational excellence with TransPerfect’s eClinical solution. Trial Interactive’s 21 CFR part 11-compliant unified eClinical platform provides solutions from site identification to eTMF archive.

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    GlobalLink

    Simplify the entire process from submission to release with GlobalLink translation management technology. Improve translation quality, expedite timelines, decrease workloads, and see significant cost savings.

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    Medical Device Solutions

    TransPerfect Medical Device Solutions is the first supplier to combine ISO 13485-, 14971-, and 9001-certified, patented language services with validated process automation technologies to meet the content management challenges of evolving regulations.

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    Clinical Research Solutions That Reduce Risk and Cost and Increase Quality and Efficiency

    Clinical Trial Management

    Simplify clinical content management and oversight, reduce operational costs by up to 40%, and accelerate therapeutic breakthroughs with our eClinical platform.

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    Pharmacovigilance and Safety Solutions

    Observe, detect, and monitor the effects of your pharmaceutical products across locations and languages with translation and call services. Ensure drug safety across your entire portfolio.

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    Clinical Outcome Assessments

    Access end-to-end consultation, from licensing to electronic clinical outcome assessment (eCOA) migration, and improve the patient and healthcare provider experience with all types of COAs.

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    Quality

    Improve compliance and reduce risk with our Trial Interactive quality management system and study team training that ensure patient safety and remove the barriers that delay product launches.

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    Patient Services

    Deploy evidence-based patient engagement tools to increase compliance and elevate product readiness. Meet the ever-growing needs of patient-centric and inclusive solutions.

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    Clinical Trial Disclosure

    We offer a full suite of clinical trial disclosure services led by transparency subject matter experts to meet requirements and publish clinical trial results with speed and quality in any language.

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    Trusted by Life Sciences Organizations Big and Small

    Navigate Through Complex Clinical Research Translation Processes With Confidence

    85% of studies experience significant delays. Streamline your operations and be the 15%. Join the 125,000+ studies across 110 countries supported by our industry-leading content solutions.

    40 %

    Reduction in R&D costs

    50 %

    Reduction in submission time

    35 %

    Reduction in patient enrollment time

    70 %

    Reduction in compliance risk

    News and Thought Leadership

    IMP Labeling Workflows That Reduce Relabeling Risk and Start-Up Delays

    Investigational medicinal product (IMP) labeling sits at the heart of clinical trial supply, impacting departments across pharmaceutical organizations, from clinical operations and regulatory affairs to quality assurance and beyond. When labeling activities are managed across multiple systems, vendors and stakeholders, teams often face avoidable rework, conflicting label text versions, delayed translations, unclear approval pathways and change control gaps that can ...

    IMP Labeling Workflows That Reduce Relabeling Risk and Start-Up Delays
    Blog

    Considerations for eCOA in Global Clinical Trials

    Regulatory Considerations for eCOA Submissions in Global Clinical Trials: What You Need to KnowWhen managing eCOA in clinical trials across multiple countries, translation, linguistic validation, and electronic implementation of Clinical Outcome Assessments (COAs) are...
    Webinar

    Xtalks | EU Clinical Trial Regulation: Latest Developments and Upcoming Opportunities

    The EU clinical trial landscape has changed significantly since Regulation (EU) No 536/2014 became applicable on January 31, 2022, and sponsors now need a clear view of how the framework is operating in practice and where it may evolve next. This webinar explores the current ...
    White Paper

    The Current State of AI in Translation for Clinical Content

    AI is reshaping how clinical trial content gets translated and localized, but in a regulated environment, speed can't come at the cost of accuracy or traceability. This white paper breaks down where AI delivers real value, where human oversight remains essential, and how to ...
    Guide

    The Veeva Vault RIM Translation Integration

    Managing multilingual regulatory submissions shouldn't mean chasing files across email threads and re-entering metadata by hand. This playbook breaks down how direct translation integration with Veeva Vault RIM eliminates manual bottlenecks, preserves compliance, and cuts ...
    Guide

    Buyer's Guide: Translation Management Integration with Veeva Vault RIM

    Translation bottlenecks, fragmented audit trails, and uncontrolled AI output aren't edge cases in regulatory operations; they're the predictable result of a poorly integrated workflow. This buyer's guide is built for regulatory leaders who need more than a file ...
    Webinar

    LifeSci Talks COA Series | Are We Sacrificing Good for Perfect in Clinical Outcome Assessment?

    In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with Stacie Hudgens, Chief Scientific and Strategy Officer at Clinical Outcome Solutions, to discuss whether the field of clinical outcome assessment has started ...

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