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.

    Fast, Compliant, Centralized Translation in Action: Lessons from AbbVie & Immunovant

    Due to high interest following our GlobalLink NEXT panel, we’re welcoming back Stacey Higgins, Associate Director, COA & Digital Implementation Team of AbbVie alongside Tihirah Harris, Sr Manager, Clinical Business Operations of Immunovant to share how and why they moved to a centralized, tech-enabled translation model—enabling faster trial timelines, cost control, and regulator-ready content. We'll also cover what’s ahead on their centralization roadmap, ...

    Fast, Compliant, Centralized Translation in Action: Lessons from AbbVie & Immunovant

    How Patients Discover Clinical Trial Websites: The Role of Localization in Search and Trust

    Could localization be the key to improving patient recruitment in clinical trials?Recruiting participants for clinical trials is a critical step in bringing new therapies and treatments to market, but despite advances in digital outreach, the industry still faces major...

    LifeSci Talks COA Series | Modernizing eCOA: Emulators, Backups, and the Future of Reporting

    In this tech-forward episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, welcomes Indira Jain-Figueroa, Product Director at Evinova, for a deep dive into the ever-evolving landscape of eCOA development. Covering everything from cross ...

    Rewriting the Rules of Informed Consent Development with AI

    How AI and Structured Content Management Are Transforming the ICF ProcessInformed consent forms (ICFs) are essential to clinical trials, serving as the primary vehicle for communicating study information to participants in a clear, ethical, and compliant manner. Given...

    Could Data Standardizations be the Silver Bullet for Faster Electronic Clinical Outcome Assessment (eCOA) Deployment?

    Choosing an electronic clinical outcome assessment (eCOA) provider is a complex process that involves a variety of different aspects including experience, scientific support and knowledge, integration capabilities, scalability, study-specific requirements, and so much more. ...

    Accelerating Pharma Labeling with Intelligent, Compliant Content

    Juggling multilingual labels across varying regions and products? Managing the updates and complying with local health authorities' requirements can be a challenge for global pharmaceutical companies, who are facing increasing pressure to streamline labelling processes and ...

    Engaging Patient Communities: A Pathway to Clinical Trial Success

    In this webinar, expert speakers from MTS Sickle Cell Foundation, Inc, Rare Disease Diversity Coalition, Black Women’s Health Imperative, and Clinical Research Associates, Inc. will focus on the critical role of patient communities in advancing clinical trials. They will ...

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