Date: Thursday, June 5, 2025
Time: 5:00–6:00 PM CT
Format: Live via Zoom
Registration: Sign up herempnadvocacy.com+4Reddit+4The Patient Story+4
Join us for the next session in the MPN Pathways: Empowered Voices in Research series, focusing on the U.S. Food and Drug Administration (FDA). This webinar will provide an overview of the FDA’s role in drug regulation, the approval process, and how MPN patients and caregivers can actively participate in shaping the future of treatments.
Speaker: Sarah Wicks, Associate at Hyman, Phelps & McNamara, P.C.
Sarah specializes in FDA regulatory and compliance matters, advocating for patient perspectives in drug development.
This session is part of a comprehensive certification program designed to educate and empower MPN patients and caregivers. All sessions are recorded and available on-demand for registered participants.
