Empowering Medical Affairs Teams with Global Content Solutions

Empowering omnichannel communications with technology-backed workflows to assist with content, localization, and management of medical affairs content. 

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Why Medical Affairs Teams Love TransPerfect

Our knowledge and experience in the medical affairs space are evidenced by our ability to create and curate strategic solutions to improve day-to-day operations and reducing administrative burdens. We have 30+ years of experience customizing these solutions. Here are some of your options:

    Medical Writing

    Ensure speed, quality, and compliance for all of your scientific communication, regulatory documentation, disclosures, and medical education.

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    Content Reuse

    Scalable, automated solutions for structured content authoring reduce the risk of human error in content reuse and drive down cycle times in producing and translating content.

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    Language/Translation Solutions

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

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    Regulatory Submissions

    Harness strategic global regulatory support throughout the product development life cycle from pre-clinical through clinical trials to marketing authorization and commercialization.

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    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 more than 200 languages 24/7/365.

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    Back-End Connectors

    Streamline translation processes with secure, automated translation workflows and storage in one ecosystem and get content to your audiences in the relevant language over 20% faster than any manual process.

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    TPT Digital

    We provide extensive market research and global expertise to develop strategic recruitment marketing plans and messaging that engage patients across all channels.

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    Chatbots

    Our team of subject matter expert linguists are experienced in localizing life sciences chatbots to better reach and engage patients, HCPs, and other stakeholders globally in more than 200 languages.

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    AI Portal to Support Real-Time Translation

    Our AI provides scalable and secure data collection, annotation, and chatbot translation services.

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    Multilingual Content Development

    Discover digital marketing solutions that help you reach, inform, and engage your global audiences.

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    Interpretation

    Use in-person, video, or phone-based interpreters for your engagements to ensure a positive experience for your participants and a productive interaction for all.

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    Deliver a Personalized And Multilingual Omnichannel Experience

    Effectively communicating and aligning key stakeholders across medical product development can be a monumental challenge. When communicating across languages, that challenge can grow even more complex. That’s why we’ve developed a suite of solutions to help simplify the process for medical affairs teams. From scientific paper development and structured content authoring to regulatory submissions and call center support, we’ve got you covered.

    Trusted by Life Sciences Organizations Big and Small

    Syneos Health
    Vertex
    Allergan
    Hologic
    IQVIA
    ICON
    Gilead
    Boehringer Ingelheim
    St Jude Medical
    AstraZeneca
    Biogen
    BMS
    PRA Health Sciences
    Sanofi logo
    Takeda logo
    Pfizer logo
    Paraxel
    NIH
    CVS Health
    Evidera/PPD
    Fulgent
    Johnson & Johnson logo
    Bayer

    Need Support with Medical Affairs Content? Let's Connect.

    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.

    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 ...