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

    Labcorp
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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.

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

    Blog

    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 answer to each other. While paper instruments might seem more flexible to deploy because they don’t require electronic implementation, there are still process considerations based on the instrument’s ...

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

    SSCPs Are Not Labeling: Compliant AI Processes for Reduced Cost & Turnaround

    In this fireside chat, TransPerfect Medical Device's President Marc Miller sits down with Dr. Keith Morel, VP of Regulatory Compliance at Qserve, to unpack a critical question facing medical device manufacturers under MDR: can you reduce the translation review process for ...
    Success Stories

    Top 10 Pharma Company Overhauls Global COA Program,Cutting Costs by 33% and Errors to Near Zero

    Inconsistent standards, stretched timelines, and limited visibility were straining a top 10 pharma company's COA program. Discover how TransPerfect Life Sciences' centralization strategy delivered 99.7% accuracy, 40% less PM oversight, and 33% cost savings across the ...
    Blog

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

    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,...
    Webinar

    How to Make Your Academy Succeed at Global Scale—Lessons Learned on What Works and What Doesn’t

    Most life sciences and MedTech companies launch a corporate academy with strong strategic intent, whether that’s executive sponsorship, a named platform, a dedicated budget, or a curriculum mapped to business goals. After launch, however, these same organizations all too often ...
    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 ...

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