With rare disease stakeholders from across the globe, 50+ exhibitors, 24+ speakers, panels, workshops, and more, The Rare Fair is the only 100% virtual event for the rare disease community.
Contact firstname.lastname@example.org to stay up-to-date on the latest news and information about The Rare Fair by joining our press list.
Do you cover rare diseases, genetics, genomics, healthcare or medicine? Health, science, and genetics reporters are invited to register now for The Rare Fair on September 1-2, 2020.
Contact Jeff Lord, at email@example.com for the Press Registration Access Code.
The focus of The Rare Fair is creating global resource networks for rare disease patients and caregivers. Reporters will hear about the latest rare disease research; have the opportunity to interact with doctors, patients, and other stakeholders to discuss what is happening right now in rare disease and view the latest products available in the Rare Tech Showcase Exhibit Hall.
Topics range from the diagnostic journey to caregiver support. Sessions include information of interest to the general public, to health professionals and to the industry/trade.
*Media Kit Coming Soon