Empowering Marketers with Global Content Solutions

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

Get in Touch
Marketing team gathered around strategy table

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.

    Learn More

    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.

    Learn More

    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. 

    Learn More

    Translation Services

    Ensure conceptual equivalence and cultural appropriateness in any language, minimizing time-to-market, mitigating risk, and ensuring compliance in global studies.

    Learn More

    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
    Johnson & Johnson logo
    Bayer
    Merck
    Moderna
    Pfizer logo
    Roche logo
    Sanofi logo

    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
    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 ...
    Guide

    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 ...

    Let Chat About Your Global Audience Engagement and Sales.

    CAPTCHA
    This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.