Empowering Marketers with Global Content Solutions

Increase your customers’ activity through digital channels with actionable data to improve ROI.

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Flexibility to Meet Your Unique Needs

Our knowledge and experience in marketing and sales is evidenced by our ability to create and curate strategic solutions to improve day-to-day operations / reducing administrative burdens. 30+ years of making these solutions for you specifically. Here are some of your options:

    Digital Marketing

    Navigate the digital marketing landscape with a full-service, central team of experts in product brand awareness and messaging. TransPerfect’s strong global presence, decades of experience in the life sciences industry, and scalable global content solutions will amplify your marketing success across all channels.

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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 over 200 languages 24/7/365.

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    Training & Development

    Training support across any platform, in 200+ languages, and any subject matter. Our team centralizes your global learning requirements and manages the administrative work, so you can roll out your content quickly and cost-effectively. 

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    Translation Services

    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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    Why Marketing and Sales Teams Love TransPerfect

    Ensuring compliance with local regulations while reaching your customers in ways they want to be communicated with is complex in an industry with ever-changing policies. Regardless of your unique goals, for scalability, growth, and success, it’s imperative that any campaigns launched are measurable with detailed analytics and insights.

    Trusted by Life Sciences Organizations Big and Small

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    Bayer
    Merck
    Moderna
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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.

    Four Years In: What the EU Clinical Trial Regulation Has (and Hasn't) Delivered

    Blog

    When the EU Clinical Trial Regulation (EU CTR No 536/2014) went live for new submissions on January 31, 2022, it promised to transform how clinical trials are authorized and conducted across Europe: a single submission, one decision, and harmonized oversight. Four years in, the reality is more nuanced. The regulatory landscape, meanwhile, is moving faster than ever. In a recent Xtalks webinar, four subject matter experts with direct experience navigating CTR and ...

    Four Years In: What the EU Clinical Trial Regulation Has (and Hasn't) Delivered
    Webinar

    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 ...
    Webinar

    The Missing Link: Why Study Design Makes or Breaks a Clinical Trial

    In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with Farrell Healion, Founder and Principal Consultant at OptiTrial, to explore why study design is so often the overlooked "missing link" in clinical ...
    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 ...

    Let Chat About Your Global Audience Engagement and Sales.

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