You can use Geneial to set up and manage rare disease patient registries without needing dedicated technical staff. The system lets you build standardized survey instruments, manage electronic consent compliant with 21 CFR Part 11, and collect longitudinal health information directly from participants. Participants can submit their health records and survey responses through a dedicated mobile application available on iOS and Android. It directly connects with existing REDCap projects to sync data without migration risks, while offering cohort analysis and gene mapping tools for medical researchers.
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