Empowering Medical Information and Pharmacovigilance Teams with Safety Technology Solutions

Ensure the safety of your patients by accelerating the time to report safety cases and communicate accurate, up-to-date information about their products.

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PV & Safety

Why Pharmacovigilance and Medical Information Teams Love TransPerfect

Our comprehensive solutions offer end-to-end support, including AI-powered case triage, literature monitoring, medical writing, and call center support. This enables faster and more accurate reporting of adverse events to regulatory bodies, reducing timelines and improving patient outcomes. Additionally, our services are designed to ensure regulatory, legal, and corporate policy adherence, reducing compliance risks for our clients.

    AI Portal for Case Triage

    Automate your translation process for faster turnaround times while also enabling your case processor to quickly prioritize incoming reports based on seriousness across 200+ languages.

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    Language/Translation Solutions

    Ensure conceptual equivalence and cultural appropriateness in any language, minimizing time-to-market, mitigating risk, and ensuring compliance in global studies.

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    eClinical

    Maintain compliance and enhance patient safety with the Trial Interactive PMSF solution. An easy-to-use, web-based format, our technology solution traffics safety notifications and distributes alerts in real-time, ensuring that sites, sponsors, and CROs remain fully apprised of the latest information and data to meet good pharmacovigilance practices (GVP) and, of course, patient safety standards.

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    Redaction

    All safety reports contain personally identifiable information (PII) of patients. Protect patient safety and privacy with our redaction services prior to regulatory review.

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    Social Media Monitoring

    Enhance patients’ real-world usage and feedback, including detecting potential adverse events, with multilingual social media monitoring.

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    Medical Writing

    When it comes to creating, managing, and translating safety content, medical writers play an integral role in protecting patient safety and adhering to strict regulations all within tight deadlines. Our team of expert medical writers have in-depth knowledge of best practices for drafting and maintaining safety content, including PSURs/PBRERs, DSURs, RMPs, and more.

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    Your Partner in Patient Safety

    With AI-powered workflows, we ensure timely and accurate reporting of Adverse Events (AEs) and Serious Adverse Events (SAEs) during clinical trials to ensure patient safety and regulatory compliance. Our streamlined processes enable rapid communication with healthcare professionals and patients to help medical information teams ensure safe and effective use of pharmaceutical products to improve patient outcomes.

    Trusted by Life Sciences Organizations Big and Small

    Chiesi
    Clario
    Fulgent
    Hologic
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    Gilead
    Bayer
    ICON
    Labcorp
    Roche logo
    Sanofi logo
    Takeda logo
    Pfizer logo

    News and Thought Leadership

    Industry insights from our experts. We have the experience and solutions you need to navigate life sciences complexity and bring breakthroughs from lab to launch.

    Digital Health Global Expansion Roadmap

    Checklist

    For digital health companies—whether startups or tech giants—successfully launching new digital health apps starts with user adoption. To ensure long-term sustainability, these apps must attract, engage, and retain a diverse user base, which means they need to be culturally and linguistically accessible to a global audience. ...

    Digital Health Global Expansion Roadmap
    Webinar

    AI in Clinical and Regulatory Content: Trends, Challenges, and Opportunities

    During this webinar, we will unveil the results of our industry survey on the role of Artificial Intelligence (AI) in clinical and regulatory content. This session will explore how AI is being evaluated and applied to search, analyze, and generate clinical and regulatory content, ...
    Guide

    Avoiding Risk in Multilingual eCOA: FDA, EMA, and ISPOR Standards

    Regulatory agencies worldwide, including the FDA, EMA, and other health authorities, require eCOA translations to be accurate, validated, and culturally adapted. ...
    Webinar

    Driving Commercial Success in Life Sciences with GenAI for Scalable Impact

    Life sciences organizations are turning to AI/ML to enhance operational efficiency, with GenAI taking center stage as a game-changer for commercial teams. Beyond process optimization, AI is accelerating the adoption of omnichannel strategies by enabling and improving precise, ...
    Webinar

    Personalized Pathways: Building an Omnichannel Ecosystem for Life Sciences

    In an increasingly globalized digital landscape, the demand for personalized content has never been greater. Listen as Joy Wendelken from Johnson & Johnson alongside Sara Green of WebMD Ignite in conversation with Dana Weber from TransPerfect Digital discuss how omnichannel ...
    Webinar

    LifeSci Talks COA Series | Data Without Interpretation is Meaningless: Unlocking Inherent Value Within the Numbers

    In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with Elizabeth (Nicki) Bush, Executive Director and Global Head of Endpoint Strategy and COA Measurement at OPEN Health Group to discuss the growing complexity of ...
    Blog

    E-Learning in Pharma: Creating & Managing Global Training Programs

    Learn how pharmaceutical companies can streamline global training programs through customizable, compliant, and engaging e-learning solutions. ...

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