RDLA’s July Legislative Webinar and In-Person Meeting
Wednesday, July 19th, 2017
12:00 – 1:00 pm ET
- Update on Healthcare Reform and ACA Replacement, Joel White, Founder and President, Horizon Government Affairs
- Reagan-Udall Foundation’s Expanded Access Navigator, June Wasser, Executive Director, Reagan-Udall Foundation
- The Food and Drug Administration Reauthorization Act (FDARA) Update, Ryan Hohman, Vice President, Public Affairs, Friends of Cancer Research
- Funding for Research Programs in the FY18 Budget, Sara Chang, Director of Policy and Advocacy, Research!America
- Orphan Product Extensions Now, Accelerating Cures and Treatments Act (OPEN ACT), Stephanie Fischer, Senior Director of Patient Engagement and Communications, EveryLife Foundation for Rare Diseases
- Upcoming Events (In-District Lobby Days and RareVoice Award Nominations), Stephanie Fischer, Senior Director of Patient Engagement and Communications, EveryLife Foundation for Rare Diseases
Once a month, RDLA convenes in person and/or over the phone to discuss legislation and developments that affect the rare disease community. The meeting/conference calls are essentially a clearing house for legislation and participation does not imply support for any of the policy proposals or legislation that are discussed or promoted.