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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    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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    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.

    The C3 Summit: Boston Recap

    The second event in our series of C3 Summits took place in Boston on May 16, 2023. We invited industry experts and leaders to discuss challenges, opportunities, and strategies in clinical trial diversity, centricity, and outcome assessments through the lens of real-world experience. In this recap of the Boston session, we will review key points from each session.  Session 1: COA/eCOA Innovations – Licensing Hiccups, Linguistic Validation, ePRO Migration, and Best ...

    The C3 Summit: Boston Recap

    How Medical Writing Can Drive Patient Engagement

    Medical writing is a critical component of the broader patient engagement landscape, establishing the foundations of communication between pharmaceutical companies and patients. The quality of medical communication can be transformational in how a patient engages with and...

    A Conversation with Dr. Elin Haf Davies of Aparito

    The rare disease space presents numerous challenges for clinical research and patient data capture. These challenges are only heightened for younger patient populations, where outcome measures and dosages need to be considered appropriately. Join Dr. Elin Haf Davies, Founder & ...

    Navigating the EU Clinical Trial Regulation Complexities - Current Challenges and Opportunities

    As the most significant change in the European Union clinical trial legislative ecosystem in 20 years, the European Union Clinical Trial Regulation 536/2014 (EU CTR) went live on January 31, 2022. The first-year transition period has now ended, and from January 31, 2023, EU ...

    How to Maximise Value and Avoid Failure During Life Sciences Dealmaking

    Please complete the form below to access the on-demand recording of our webinar. A fantastic expert panel of life sciences dealmaking veterans from AstraZeneca and Merck, with 100 years' collective experience, share their insights on key dealmaking strategies, best practices ...

    Centralizing Global Content Solutions for Medical Affairs

    With a rapidly evolving landscape and the introduction of new technologies and emerging therapeutics, medical affairs professionals are tasked with remaining in lockstep with the latest industry developments. From a content perspective, this means not only maintaining clear...

    Automation for MDR & IVDR: A Three-Part Seminar - Part 3: EnCompass Step by Step: A Detailed View of the Content Automation Solution to Meet MDR & IVDR Requirements

    Part 3: EnCompass Step by Step: A Detailed View of the Content Automation Solution to Meet MDR & IVDR Requirements ...

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