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

    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 translation timelines by up to 90%. Whether you're submitting across five markets or fifty, learn what it takes to build a workflow that scales without the operational fire drills. ...

    The Veeva Vault RIM Translation Integration

    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 ...

    Libraries in Clinical Outcome Assessments: How Valuable Are They—and Are They the Panacea They’re Claimed to Be?

    Speed, cost, and quality are competing priorities in eCOA localization. Discover why translation libraries alone aren't enough, and what combination of proactive licensing, automation, and integrated technology can transform your deployment timelines. ...

    Is AI Ready to Transform COA Development?

    AI is reshaping clinical development, but its greatest value may lie not in replacing human expertise, but rather in augmenting it. Across the drug development pipeline, AI is helping teams analyze vast datasets faster, identify promising compounds earlier, and uncover...

    Five Domains the FDA Wants You to Measure in PROs for Cancer—and Why Translation Affects All of Them

    In a recent "LifeSci Talks" episode, TransPerfect Global Practice Leader Mark Wade and Signant Health VP and eCOA Scientist Bill Byrom PhD discussed how new FDA guidance is reshaping how sponsors approach patient-reported outcomes (PROs) in cancer clinical trials. PROs...

    Xtalks | Improve Recruitment Outcomes Through More Diverse Clinical Trials

    Since the advent of artificial intelligence (AI), medical device manufacturers have been early adopters for product enhancements. Now, manufacturers are evaluating their regulated content and other production processes for suitable applications of AI and automation technology. ...

    Potential Impact of the EU Biotech Act Proposal on Clinical Trial Activities

    The European Commission’s proposed Biotech Act introduces changes that could reshape how clinical trials are approved and managed across the EU. While the broader package spans multiple areas of the health ecosystem, proposed updates to the EU Clinical Trial Regulation (EU...

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