Watch this on-demand webinar to hear industry experts from Worldwide Clinical Trials, Raremark, patient advocacy groups, and pharmaceuticals discuss rare disease community connections during a global pandemic. Learn what this means for the healthcare ecosystem, the role of patient advocacy groups, and how technology is pivoting to accommodate connectivity, socialization, and real-world evidence. Are win-win scenarios possible in times of uncertainty?
Leveraging Rare Disease Community Connections in (and after) a Time of Change
Fostering rare disease research progress through community connections
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