Reduce Friction in Your Clinical Research to Accelerate Development Timelines

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

Streamline My Study
Mold

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.

    Learn More

    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.

    Learn More

    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.

    Learn More

    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.

    Learn More

    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.

    Learn More

    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.

    Learn More

    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.

    Learn More

    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.

    Learn More

    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.

    Learn more ›

    Pharmacovigilance and Safety

    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.

    Learn more ›

    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.

    Learn more ›

    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.

    Learn more ›

    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.

    Learn more ›

    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.

    Learn more ›

    Trusted by Life Sciences Organizations Big and Small

    Boehringer Ingelheim
    Moderna
    Novartis
    Pfizer logo
    Paraxel
    P&G
    Takeda logo
    Sanofi logo
    Gilead
    Vertex
    AstraZeneca
    Biogen
    BMS
    Johnson & Johnson logo
    Merck

    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 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. ...

    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...

    How to Select the Right Regulatory Writing Company for Your Organization's Needs

    In a landscape defined by ever-evolving global guidelines from health authorities, many life sciences organizations’ clinical and regulatory teams face challenges in navigating the regulatory affairs writing and document submission process. Adhering to strict rules while...

    5 Essential Use Cases for Generative AI and Machine Translation in Regulatory Content Submissions

    Moving a drug from development, through clinical trials, to eventually the market involves many critical content pieces and challenges along the way.   According to research commissioned by Genpact, 72% of senior executives across the life sciences industry cited...

    Ready to launch and manage clinical trials faster?