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.

    IMP Labeling Workflows That Reduce Relabeling Risk and Start-Up Delays

    Investigational medicinal product (IMP) labeling sits at the heart of clinical trial supply, impacting departments across pharmaceutical organizations, from clinical operations and regulatory affairs to quality assurance and beyond. When labeling activities are managed across multiple systems, vendors and stakeholders, teams often face avoidable rework, conflicting label text versions, delayed translations, unclear approval pathways and change control gaps that can ...

    IMP Labeling Workflows That Reduce Relabeling Risk and Start-Up Delays
    Event

    C3 Summit 2026 - London

    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 ...
    Blog

    Considerations for eCOA in Global Clinical Trials

    Regulatory Considerations for eCOA Submissions in Global Clinical Trials: What You Need to KnowWhen managing eCOA in clinical trials across multiple countries, translation, linguistic validation, and electronic implementation of Clinical Outcome Assessments (COAs) are...
    Webinar

    Xtalks | EU Clinical Trial Regulation: Latest Developments and Upcoming Opportunities

    The EU clinical trial landscape has changed significantly since Regulation (EU) No 536/2014 became applicable on January 31, 2022, and sponsors now need a clear view of how the framework is operating in practice and where it may evolve next. This webinar explores the current ...
    Checklist

    Veeva RIM TMS Integration Checklist

    If your regulatory team is still downloading documents from Veeva Vault, managing translation requests by email, or tracking submissions in spreadsheets, there's a better way. Reduce complexity, close compliance gaps, and shorten your submission cycle times with this ...
    White Paper

    The Current State of AI in Translation for Clinical Content

    AI is reshaping how clinical trial content gets translated and localized, but in a regulated environment, speed can't come at the cost of accuracy or traceability. This white paper breaks down where AI delivers real value, where human oversight remains essential, and how to ...
    Guide

    The Veeva Vault RIM Translation Integration

    Managing multilingual regulatory submissions shouldn't mean chasing files across email threads and re-entering metadata by hand. This playbook breaks down how direct translation integration with Veeva Vault RIM eliminates manual bottlenecks, preserves compliance, and cuts ...