360° Workflow Solutions for Your Medical Affairs Initiatives

Choose omnichannel solutions that improve the quality, timeliness, cost, and effectiveness of multilingual medical affairs content.

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AI-powered workflows

Solutions that Create Impactful Content for Global Audience

Evolve your medical affairs operations into a global, integrated model with AI-powered translation technology, expert language services, and global support.

    Veeva Connector (MLR Workflows)

    Reduce the manual effort of copying and pasting content into and out of other technologies, like Veeva, with automation. Keep all content in one ecosystem to streamline the MLR review process.

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    Content Reuse (SCMS)

    Manage your content processes in an intuitive authoring environment that enables you to more effectively reuse content, propagate changes, enable omnichannel delivery, and streamline the review and approval process.

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    Call Center Support

    Provide a clear and comprehensive customer service support experience that offers in-language guidance and speeds up the creation and communication of critical information to patients and HCPs.

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    Medical Writing

    Deliver first-class medical writing with analysis, creation, translation, and SME support for your clinical trial and research information. Know your content is clear, concise, and follows global regulations.

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    Literature & Social Media Monitoring

    Meet with experts to review keyword requirements, search terms, and localization. Use technology to consolidate literature into one dataset for search strings to be applied, centralize review of literature, and decide actions that are required.

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    Digital Marketing

    Gain strategic guidance on your omnichannel digital marketing efforts and website localization with our TPT Digital solution. Drive visibility to global marketing campaigns and create targeted messaging based on the customer journey.

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    Localization/Adaption

    Utilize real-time data about individual markets and regional native languages to create hyper-specific content. Manage content localization in 200+ languages, reduce project management time, and mitigate risks.

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    Chatbots

    Expand your channels of communication with culturally appropriate chatbots. Disseminate med affairs information through TransPerfect’s DataForce technology, an AI solution that uses ML to improve responses over time.

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    AI Portal for Real-Time Translation

    Provide a cost-effective and secure document translation solution for short-turnaround projects. Using machine translations, understand content quickly to generate and communicate accurate scientific information.

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    Omnichannel Marketing in Med Affairs

    The Benefits of A Comprehensive Medical Affairs Solution

    Even simple language changes to medical affairs content can significantly impact the effectiveness of global messaging. Handle delicate subject matters with care with TransPerfect.

    • Eliminate the need for multiple vendors with content creation and localization under one roof.
    • Get critical information to audiences faster with high-quality content development and translation support.
    • Expand your channels of communication—including sophisticated chatbots, websites, videos, and more.
    • Enable a seamless flow and exchange of information among internal and external medical stakeholders with our fully integrated knowledge management system.

    Trusted by Life Sciences Organizations Big and Small

    Join TransPerfect's community of more than 1,000 life sciences organizations, including pharma, biotech, CROs, IRBs, and agencies.

    Improving Global Medical Affairs Management by the Numbers


    90 %

    Reduction in internal project management

    50 %

    Faster customer response times

    50 %

    Increase in content reuse

    25 %

    Saved on content development costs

    News and Thought Leadership

    Our industry experts have in-depth understanding of the challenges, requirements, and goals for medical affairs teams in reaching global audiences.

    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 today’s eCOA capabilities or institutional habit. Paper is often framed as the “gold standard,” yet paper-based patient-reported outcome data can be incomplete, error-prone and difficult to ...

    XTalks | eCOA: Has It Lived Up to the Promise? A Realistic Assessment for Today's Trials

    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 ...

    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,...

    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 ...

    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 ...

    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 ...

    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 ...

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