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    Meet Veristat at the 2026 AMWA Medical Writing & Communication Conference

    Advancing Medical Writing and Regulatory Submissions in an Increasingly Complex Environment  

    November 2026 | Exhibit Hall, Table # 13

    Veristat is pleased to participate in the 2026 AMWA Medical Writing & Communication Conference, bringing together medical writing, regulatory, and communications professionals to discuss emerging challenges, evolving technologies, and best practices across the industry.

    As regulatory applications become more complex and AI reshapes medical writing and editing, organizations need the right expertise, processes, and strategies to deliver high-quality, submission-ready documentation. Veristat brings deep experience in regulatory science, medical writing, and global submissions to help sponsors navigate these demands and advance development programs toward approval.

    Join Our Expert-Led Sessions

    Veristat experts will share their perspectives in three conference sessions:

    As Regulatory Applications Become More Complex, How Do We Still Deliver Successfully?
    November 5 | 9:30–10:30 AM
    Brenda Taylor, Director, Global Submissions
    Mark Bowlby, Senior Director, Global Submissions
    Steve Sibley, VP, Global Submissions
    View Session

    The AI-Augmented Medical Editor: A 2027 Job Description
    November 6 | 10:45–11:45 AM
    Featuring Demetrius Carter, Life Sciences Executive, Veristat, alongside industry panelists.
    View Session

    From Author to Architect: Leading and Operating a High-Impact Medical Writing Function
    November 6 | 3:00–4:00 PM
    Heather Graham, VP, Regulatory Science and Medical Affairs
    View Session

     

    Meet With Us

    Visit Veristat at Table #13 in the exhibit hall to discuss your medical writing, regulatory strategy, and global submission needs. Our team looks forward to sharing how integrated expertise can help strengthen submission readiness and advance your development goals. 

    Schedule a Meeting in Advance

    Complete the form on this page to reserve time with our team. We welcome the opportunity to learn about your upcoming programs and explore how Veristat can support your development strategy. 

    Our Expertise

    Whether you're launching a first-in-human study or navigating complex regulatory pathways, Veristat delivers integrated expertise and personalized support across the development lifecycle:

    • Full-Service Clinical Development Solutions
    • Global Regulatory Strategy & Submissions
    • Clinical Operations Excellence
    If you’ll be at the meeting, let’s make time to discuss how we can help move your programs forward.

     

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