RDLA’s June Legislative Webinar and In-Person Meeting


Wednesday, June 14th, 2017
12:00 – 1:00 pm ET

440 First Street Northwest, Suite 430
Washington, DC 20001

  • Latest Update on FDA Hiring Freeze and Funding for FY 18
    • Steve Grossman, Deputy Executive Director, Alliance for a Stronger FDA
  • Newborn Screening Updates and the Impact of the Presidential Budget
    • Rebecca Abbott, Deputy Director of Federal Affairs for Public Health, March of Dimes
  • RDLA Program Director Introduction
    • Sabah Bhatnagar, RDLA Program Director, EveryLife Foundation
  • Orphan Product Extensions Now, Accelerating Cures and Treatments Act (OPEN ACT) and Florida Newborn Screening Legislation
    • Max Bronstein, Chief Advocacy and Science Policy Officer, EveryLife Foundation for Rare Diseases
  • Upcoming RDLA Events (RARE on the Road and In-District Lobby Days)
    • Julia Jenkins, Executive Director, EveryLife Foundation for Rare Diseases

Agenda is OPEN. Please submit possible agenda items to Hannah (HClauson@everylifefoundation.org).

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.

Filed Under: Community Events, Rare Community

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