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.

    The Total Economic Impact of TransPerfect GlobalLink for Life Sciences

    White Paper

    TransPerfect commissioned Forrester Consulting to conduct a Total Economic Impact™ (TEI) study and examine the return on investment (ROI) enterprises may realize by deploying GlobalLink. The objective of the framework is to identify the cost, benefit, flexibility, and risk factors that affect the investment decision. Forrester took a multistep approach to evaluate the impact that GlobalLink can have on an organization. The purpose of this study is to provide readers ...

    The Total Economic Impact of TransPerfect GlobalLink for Life Sciences
    Webinar

    AI and MT for PV and Safety Office Hours - 4/23/25

    Welcome to TransPerfect Life Sciences' AI and MT Ask an Expert Office Hours. In these sessions, we provide an opportunity for our community to submit their pressing questions for our experts to answer live, in the company of your industry peers. If you are looking for some ...
    Webinar

    Ask an Expert Office Hours: Website Localization for Patient Recruitment - 4/24/25

    This session focuses on Website Localization for Patient Recruitment. Tackle your toughest patient recruitment and engagement challenges with free, no-strings-attached advice from TransPerfect's web localization and AI experts—no cost, no sales pitch, just solutions! ...
    Checklist

    Digital Health Global Expansion Roadmap

    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 ...
    Client Story

    Smith & Nephew Saves $200k Annually While Meeting MDR & IVDR Stringent Vigilance Requirements

    Part of TransPerfect's GlobalLink suite of productivity applications, GlobalLink Now is a simple, but powerful way to access secure, customized AI. The system has an intuitive UI for sign on and engagement, making the application easy to use and adopt. ...
    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. ...

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