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.

    Buyer's Guide: Translation Management Integration with Veeva Vault RIM

    Translation bottlenecks, fragmented audit trails, and uncontrolled AI output aren't edge cases in regulatory operations; they're the predictable result of a poorly integrated workflow. This buyer's guide is built for regulatory leaders who need more than a file-moving connector between their TMS and Veeva Vault RIM. Inside, you'll find a detailed evaluation framework, a vendor due diligence checklist, and a breakdown of the compliance, AI ...

    Buyer's Guide: Translation Management Integration with Veeva Vault RIM
    Blog

    AI Governance in Medical Information: What "Human-in-the-Loop" Actually Requires

    These days, you can't have a conversation about AI in life sciences without someone invoking "human-in-the-loop." It's become so expected that leaving it out feels like a red flag—a signal that AI governance hasn't been fully considered. The problem isn't the phrase...
    Event

    C3 Summit 2025 - 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 ...
    White Paper

    Libraries in Clinical Outcome Assessments: How Valuable Are They—and Are They the Panacea They’re Claimed to Be?

    Speed, cost, and quality are competing priorities in eCOA localization. Discover why translation libraries alone aren't enough, and what combination of proactive licensing, automation, and integrated technology can transform your deployment timelines. ...
    Blog

    From Reactive to Strategic: How AI Is Transforming Medical Information Contact Centers

    IntroductionFor decades, Medical Information (MI) has been an essential function within pharma, but largely a reactive one. This is especially true in medical information contact centers, which serve as the first line of support for HCPs and patients. When someone has a...
    Blog

    Is AI Ready to Transform COA Development?

    AI is reshaping clinical development, but its greatest value may lie not in replacing human expertise, but rather in augmenting it. Across the drug development pipeline, AI is helping teams analyze vast datasets faster, identify promising compounds earlier, and uncover...
    Blog

    Five Domains the FDA Wants You to Measure in PROs for Cancer—and Why Translation Affects All of Them

    In a recent "LifeSci Talks" episode, TransPerfect Global Practice Leader Mark Wade and Signant Health VP and eCOA Scientist Bill Byrom PhD discussed how new FDA guidance is reshaping how sponsors approach patient-reported outcomes (PROs) in cancer clinical trials. PROs...