European survey about Patients´ unmet need in medical research

A survey, organized by the working group Research and Science of the European Reference Network on rare endocrine conditions (Endo-ERN) is being conducted. The aim of this survey is to gain the views and experiences of people living with rare endocrine disorders about the research they think should be prioritized related to their disease within European countries. Patients, parents, and relatives can participate in this study by following this link.