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    Meet Veristat at the 4th International Conference on Rare Diseases and Orphan Drugs

    Advancing Rare Disease Therapies Through Complex Development Challenges 

    October 22-23, 2026 | Barcelona

    Veristat is pleased to attend the Rare Diseases and Orphan Drugs conference, bringing together industry experts, researchers, and innovators focused on advancing treatments for patients with rare conditions. With small patient populations, limited natural history data, and complex regulatory pathways, rare disease development requires thoughtful strategies and specialized expertise at every stage.

    We look forward to exchanging perspectives with sponsors and rare disease innovators on approaches to trial design, patient recruitment, evidence generation, and regulatory planning. Veristat brings integrated expertise across clinical development, biostatistics, and regulatory science to help sponsors address these challenges, strengthen their development strategies, and advance promising therapies toward approval.

    Meet With Us

    Connect with us at the event to explore how Veristat’s scientific leadership and focused capabilities can help advance your clinical and regulatory milestones.

    Balma Gil, Business Development Director 
    Jayne Hunt, Regulatory Affairs Director

    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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