360° Workflow Solutions for Your Medical Affairs Initiatives

Choose omnichannel solutions that improve the quality, timeliness, cost, and effectiveness of multilingual medical affairs content.

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AI-powered workflows

Solutions that Create Impactful Content for Global Audience

Evolve your medical affairs operations into a global, integrated model with AI-powered translation technology, expert language services, and global support.

    Veeva Connector (MLR Workflows)

    Reduce the manual effort of copying and pasting content into and out of other technologies, like Veeva, with automation. Keep all content in one ecosystem to streamline the MLR review process.

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    Content Reuse (SCMS)

    Manage your content processes in an intuitive authoring environment that enables you to more effectively reuse content, propagate changes, enable omnichannel delivery, and streamline the review and approval process.

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    Call Center Support

    Provide a clear and comprehensive customer service support experience that offers in-language guidance and speeds up the creation and communication of critical information to patients and HCPs.

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    Medical Writing

    Deliver first-class medical writing with analysis, creation, translation, and SME support for your clinical trial and research information. Know your content is clear, concise, and follows global regulations.

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    Literature & Social Media Monitoring

    Meet with experts to review keyword requirements, search terms, and localization. Use technology to consolidate literature into one dataset for search strings to be applied, centralize review of literature, and decide actions that are required.

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    Digital Marketing

    Gain strategic guidance on your omnichannel digital marketing efforts and website localization with our TPT Digital solution. Drive visibility to global marketing campaigns and create targeted messaging based on the customer journey.

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    Localization/Adaption

    Utilize real-time data about individual markets and regional native languages to create hyper-specific content. Manage content localization in 200+ languages, reduce project management time, and mitigate risks.

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    Chatbots

    Expand your channels of communication with culturally appropriate chatbots. Disseminate med affairs information through TransPerfect’s DataForce technology, an AI solution that uses ML to improve responses over time.

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    AI Portal for Real-Time Translation

    Provide a cost-effective and secure document translation solution for short-turnaround projects. Using machine translations, understand content quickly to generate and communicate accurate scientific information.

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    Omnichannel Marketing in Med Affairs

    The Benefits of A Comprehensive Medical Affairs Solution

    Even simple language changes to medical affairs content can significantly impact the effectiveness of global messaging. Handle delicate subject matters with care with TransPerfect.

    • Eliminate the need for multiple vendors with content creation and localization under one roof.
    • Get critical information to audiences faster with high-quality content development and translation support.
    • Expand your channels of communication—including sophisticated chatbots, websites, videos, and more.
    • Enable a seamless flow and exchange of information among internal and external medical stakeholders with our fully integrated knowledge management system.

    Trusted by Life Sciences Organizations Big and Small

    Join TransPerfect's community of more than 1,000 life sciences organizations, including pharma, biotech, CROs, IRBs, and agencies.

    Improving Global Medical Affairs Management by the Numbers


    90 %

    Reduction in internal project management

    50 %

    Faster customer response times

    50 %

    Increase in content reuse

    25 %

    Saved on content development costs

    News and Thought Leadership

    Our industry experts have in-depth understanding of the challenges, requirements, and goals for medical affairs teams in reaching global audiences.

    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

    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 ...

    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 ...

    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. ...

    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...

    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,...

    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 ...

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