News & Updates

The Children’s Rare Disease Network is giving away a rare disease research registry valued up to $50,000. RemedyMD has spent the last 10 years and millions developing this meta-registry technology so that rare disease researchers can accelerate their efforts when they otherwise would not have had the resources or funds to on their own. RemedyMD has donated access to this formatted dataset and will be announcing details at the upcoming free rare disease webinar this June 22nd at 2 PM (EDT). Registries 2.0 – Using Clinical Data to Accelerate Rare Disease Research

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