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 Ultimate Clinical Trial Translations Checklist

    Clinical product development is an elaborate endeavor executed through a complex web of processes that are in large part accomplished through various document and communication work streams. These work streams can represent a significant source of cost, risk, and time. When a study operates across cultures, countries, and continents, these pain points of cost, risk, and time are compounded by the addition of translation and localization requirements. Study teams ...

    The Ultimate Clinical Trial Translations Checklist

    CCMS: A Good Fit for Pharmaceutical and Clinical Research Organizations?

    Kaarin Gordon discusses the choices and challenges for efficient content reuse facing Pharmaceutical and Clinical Research Organizations. What they want is a set of tools and platforms for easy content reuse, automatic propagation of changes from a single source, and content ...

    Omnichannel Marketing for the Pharmaceutical Industry

    With rapid globalization and expanded marketing efforts, pharmaceutical organizations are discovering that pivoting from multichannel marketing to omnichannel marketing is key to revolutionizing patient engagement. Through tailored experiences across relevant channels, your teams ...

    LifeSci Talks COA Series | The Future of Capturing Patient Data in Clinical Trials: DCTs, Site Staff Burden, and Regulation Considerations with Paul O'Donohoe

    Mark Wade interviews Paul O'Donohoe, Senior Director of Product for eCOA and COA at Medidata. They delve into the challenges and opportunities of adopting decentralized clinical trials (DCTs) and explore topics such as mixed modalities for data capture, patient burden, site ...

    Walking the Tightrope: Navigating Patient Centricity and Burden in Modern Clinical Trials

    Over the past few decades, clinical trials have witnessed remarkable developments - but they are not without challenges. Dropout rates of up to 20% indicate that patient burden and engagement remain key areas of concern. In response to this, sponsors, healthcare providers,...

    Health Canada's XML Mandate: Pioneering the Future of Pharmaceutical Content

    In 2019, Health Canada initiated a significant process to transition all product monograph templates into a more advanced and structured XML format. This move by the regulatory authority has raised several questions for Canadian pharmaceutical organizations' regulatory and...

    Leveraging Technology and Bridging Gaps for Enhanced Clinical Data Management

    Introduction: In the field of clinical research, a robust data management process is essential for driving success. Efficiently handling vast amounts of data, ensuring accuracy and consistency, and extracting meaningful insights are vital, particularly in the case of global...

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