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.

    Your Multilingual Trial Site SEO Success Checklist

    Multilingual trial SEO is critical to ensure that patients and HCPs can actually find and act on your trial content in their language. This checklist walks clinical trial teams through five essentials:… ...

    Your Multilingual Trial Site SEO Success Checklist
    Blog

    Clinical Trials Translation Management: A Scalable Workflow for Faster Enrollment

    When it comes to clinical trials, website localization isn’t just about translating words into other languages. It’s about designing a governed, repeatable workflow that keeps every multilingual page accurate, reviewable, and in sync as content changes. This ensures patients,...
    Blog

    7 Workflow Hacks for Smarter Clinical Trial Localization

    Imagine this: a director of clinical operations at a mid-size pharma needs better regional recruitment to hit aggressive enrollment deadlines. So, they push to launch the company website in nine languages at once. The moment the request lands, the clinical compliance manager...
    Webinar

    LifeSci Talks COA Series | Building Fit-for-Purpose PRO Instruments: Focused Modern Measures Over General Instruments

    In this episode of LifeSci Talks, Mark Wade, Global Practice Leader & COA SME at TransPerfect Life Sciences, is joined by Katja Rudell, VP of Patient-Centered Outcomes at Kielo Research, to take a behind-the-scenes look at the reality of patient-centered instrument ...
    White Paper

    How Medical Communications Teams Can Scale Reviews Without Sacrificing Speed

    Medical communications teams are under mounting pressure to review more content than ever before without adding headcount or increasing risk. This white paper outlines five pillars for rethinking MLR workflows, from modular content and tiered reviews to automation and governance. ...
    Checklist

    Patient Recruitment: Clinical Research's Costliest Bottleneck

    Patient recruitment is the costliest bottleneck in clinical research. Learn proven strategies to reduce study delays, optimize enrollment, and cut regrettable spend. ...
    White Paper

    From Draft to Deployment: Creating Global-Ready Content from the Start

    Clinical, regulatory, and commercial teams all rely on the same content, yet often work in siloes. This white paper examines the real cost of disconnected content strategies and why localization should be treated as a strategic input, not a final step. Discover how global-ready ...

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