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
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    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.

    Integrating eCOAs and Digital Health for Patient-Centric Trials

    Blog

    A New Era of Patient-First Design  Clinical research is undergoing a fundamental transformation as technology takes on a larger role in how trials are designed and executed. This shift is not simply about digitizing paper-based processes, but about creating ecosystems that allow patients to engage with research in ways that feel natural and supportive. At the center of this evolution is the principle of patient-first design, which ensures that participants are ...

    Integrating eCOAs and Digital Health for Patient-Centric Trials
    Success Stories

    Opening Doors Worldwide: Launching a Top 10 Pharma’s Careers Site in 15 Languages

    With an ambitious global rollout deadline and limited internal bandwidth, this top 10 pharma company needed a smarter way to scale localization. Learn how automation and streamlined workflows helped transform the candidate experience across 15 markets, without slowing down speed ...
    Success Stories

    From Local to Global: How a Top 10 Pharma Leader Delivered Trial Access in Nine Languages

    Discover how one of the world’s leading pharmaceutical companies made its clinical trial website accessible to global patients, but faced tight timelines, limited resources, and shifting systems. See how the team overcame these challenges to launch a multilingual site that set a ...
    Webinar

    Optimizing Technology and Automation for Digital Health Products

    Accurate and culturally appropriate translation of clinical outcome assessments (COAs), including patient-reported outcome measures, is essential to ensuring reliable data in multinational trials. Foundations of Clinical Outcome Assessment Localization will provide a practical ...
    Webinar

    Foundations of Clinical Outcome Assessment Localization

    Accurate and culturally appropriate translation of clinical outcome assessments (COAs), including patient-reported outcome measures, is essential to ensuring reliable data in multinational trials. Foundations of Clinical Outcome Assessment Localization will provide a practical ...
    Webinar

    Life Sciences Learning Trends - Office Hours Q&A

    Join the TransPerfect Learning team for an interactive virtual C3 Study Session, focused on the latest commercial learning trends transforming the life sciences industry. Whether you attended LTEN 2025 or are simply passionate about advancing learning & development in your ...
    Webinar

    AI in Pharmacovigilance: A Catalyst for Progress or a Tradeoff to Human Potential?

    In an environment as high stakes as pharmacovigilance, AI is not just about technology implementation; it's about balancing compliance, patient safety, and developmental breakthroughs. In this session, industry experts Dr. Siva Kumar Buddha of Amgen alongside TransPerfect& ...

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