Event
World Orphan Drug Congress EU
Connect with us at World Orphan Drug Congress EU!
Join us at booth #10311 at the World Orphan Drug Congress EU, where leaders in rare disease innovation come together to accelerate the future of orphan drug development. Let’s connect on how our deep rare disease expertise and patient-first approach can support your next breakthrough.
Visit us for our session:
Embracing the Future of Clinical Trials to Transform Rare Disease Clinical Studies
Date: October 28, 5:10 PM
Speaker: Corinne Blanchet, MS, Executive Director, Program Delivery, Rare Disease & Pediatrics
Request a Meeting
During a meeting with our team, we’ll discuss your unique challenges and ways we can tailor our end-to-end support and experience to address the needs of your rare disease program:
- Extensive experience across 280+ rare and genetic disorder studies
- Innovative study design and endpoint selection
- Partnership with trial participants
- Focused regulatory guidance
Fill out the form to schedule a time to meet with our team!
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