ERCAL is a multi-stakeholder Foundation in Latin America and the Caribbean (LAC) consisting of expert individuals and organizations that promote and work to improve the lives of people living with rare diseases and their families.
Formed by experts and patient organizations, we are a regional cooperation alliance that integrates the participation of all stakeholders committed to establishing favorable regulatory contexts, and develop activities with actionable plans to improve the quality of life of people living with a rare disease and their families in a joint and articulated effort.
Our vision is to be the alliance of reference for the entire rare disease ecosystem in the LAC region that integrates and commits essential stakeholders, such as academia, physicians, medical societies, governmental or non-governmental organizations, private companies and patient advocacy groups, to cooperate for a more equitable environment.