NORD Drives Rare Disease Progress Through Patient-Powered Data With IAMRARE™ Registry Members
Written by Laura Mullen on November 10, 2020
Washington, DC, November 10, 2020—This year, in conjunction with its rare disease community partners, the National Organization for Rare Disorders (NORD®) continued to drive research and innovation through the IAMRARE™ registry program. Having launched its first study in 2014, today IAMRARE
