Natural History Studies and Registries in the Development of Rare Disease Treatments

This in-person and virtual public workshop will bring together rare disease patient advocates, academic researchers, regulated industry, and other key stakeholders to discuss considerations for the use of natural history study and registry data in rare disease drug development programs.

Find more information at https://reaganudall.org/news-and-events/events/natural-history-studies-and-registries-development-rare-disease-treatments