Empowering Medical Affairs Teams with Global Content Solutions

Empowering omnichannel communications with technology-backed workflows to assist with content, localization, and management of medical affairs content.

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Why Medical Affairs Teams Love TransPerfect

Our knowledge and experience in the medical affairs space are evidenced by our ability to create and curate strategic solutions to improve day-to-day operations and reducing administrative burdens. We have 30+ years of experience customizing these solutions. Here are some of your options:

    Medical Writing

    Ensure speed, quality, and compliance for all of your scientific communication, regulatory documentation, disclosures, and medical education.

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    Content Reuse

    Scalable, automated solutions for structured content authoring reduce the risk of human error in content reuse and drive down cycle times in producing and translating content.

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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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    Regulatory Submissions

    Harness strategic global regulatory support throughout the product development life cycle from pre-clinical through clinical trials to marketing authorization and commercialization.

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    Call Center Support

    Our state-of-the-art technology, secure contact centers, expert interpreters, and support agents enable you to access a medical subject matter expert interpreter within seconds—in more than 200 languages 24/7/365.

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    Back-End Connectors

    Streamline translation processes with secure, automated translation workflows and storage in one ecosystem and get content to your audiences in the relevant language over 20% faster than any manual process.

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    TPT Digital

    We provide extensive market research and global expertise to develop strategic recruitment marketing plans and messaging that engage patients across all channels.

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    Chatbots

    Our team of subject matter expert linguists are experienced in localizing life sciences chatbots to better reach and engage patients, HCPs, and other stakeholders globally in more than 200 languages.

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    AI Portal to Support Real-Time Translation

    Our AI provides scalable and secure data collection, annotation, and chatbot translation services.

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    Multilingual Content Development

    Discover digital marketing solutions that help you reach, inform, and engage your global audiences.

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    Interpretation

    Use in-person, video, or phone-based interpreters for your engagements to ensure a positive experience for your participants and a productive interaction for all.

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    Deliver a Personalized And Multilingual Omnichannel Experience

    Effectively communicating and aligning key stakeholders across medical product development can be a monumental challenge. When communicating across languages, that challenge can grow even more complex. That’s why we’ve developed a suite of solutions to help simplify the process for medical affairs teams. From scientific paper development and structured content authoring to regulatory submissions and call center support, we’ve got you covered.

    Trusted by Life Sciences Organizations Big and Small

    Need Support with Medical Affairs Content? Let's Connect.

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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.

    The 5-Step AI Readiness Checklist for Medical Device Manufacturers

    Only one in four manufacturers using process AI say it's meeting expectations. The gap between those results and the rest comes down to preparation. This checklist is built from patterns shared by manufacturers that are seeing results, along with the gaps most commonly found among those that aren't. ...

    The 5-Step AI Readiness Checklist for Medical Device Manufacturers
    Webinar

    XTalks | How MI, PV & Regulatory Collaborate on Signals, Labeling, Crisis Response and AI

    Medical Information (MI), Pharmacovigilance (PV) and Regulatory Affairs (RA) each play distinct but deeply interconnected roles in ensuring that therapeutics are safe, accurately labeled and compliantly communicated to healthcare professionals and patients. Yet in practice, the ...
    Event

    C3 Summit 2026 - San Francisco

    Conversations on Clinical Content, C3 Summit is part of a series of events hosted by TransPerfect Life Sciences featuring sessions with expert panels discussing present challenges, strategies, and innovations, as well as insights into future advancements, from R&D to ...
    Webinar

    LifeSci Talks COA Series | Nothing Remains the Same: Why Measures Have to Evolve

    In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with RJ Wirth, CEO and Consulting Psychometrician at Vector Psychometric Group, to talk about why the measures we rely on are living things rather than fixed artifacts. ...
    Blog

    Regulatory Considerations for Paper COA Translations | What You Need to Know

    Collecting data for a global clinical trial on paper COAs or managing a mixed-mode study that combines both paper and electronic formats means satisfying multiple regulatory bodies before a single patient enrolls. None of these entities operate on the same timeline or...
    Blog

    When "How Does the Patient Feel?" Became a Regulatory Question

    For decades, clinical trials were built around things you could measure with a machine: tumor shrinkage on a scan, laboratory values, and disease progression. These hard, objective endpoints were the backbone of drug approval. The patient's own account of how they felt,...
    Webinar

    XTalks | eCOA: Has It Lived Up to the Promise? A Realistic Assessment for Today's Trials

    Despite two decades of technological advancement, the debate between paper and electronic clinical outcome assessments (eCOA) remains unresolved. This webinar revisits the assumptions that continue to shape data collection strategies and examines whether current practice reflects ...