An innovative platform for collecting data from rare disease patients.
Headquarter
Londra
Typology
Early Stage
Management
Julie Walters
Raremark: context and impact
In the rare disease market, information sharing is scarce, patients are often isolated from each other, and research centers and specialists struggle to gather data and information needed to develop new drugs to treat the diseases.
RareMark has created a social network for rare disease patients, allowing families to keep update with the latest research and research centers and to obtain anonymous data for the development of drugs needed to treat rare diseases.
