National plan for rare diseases: Czech Republic

Please find documents on/ relevant to the national strategy, action plans for rare diseases and EUROPLAN conferences in the Czech Republic listed below:

  1. Czech Republic_RD National Strategy_2010-2020_Czech
  2. Czech Republic_RD National Strategy_2010-2020_English
  3. Czech Republic_RD Action Plan_2012-2014_Czech
  4. Czech Republic_RD Action Plan_2012-2014_English
  5. Czech Republic_RD Action Plan_2015-2017_Czech
  6. Czech Republic_RD Action Plan_2015-2017_English
  7. EUROPLAN_2017_Czech Republic_Round Table_Report_English

National contact:
Česká asociace pro vzácná onemocnění (ČAVO)
Rare diseases Czech Republic

Page created: 19/03/2019
Page last updated: 30/04/2019
The voice of rare disease patients in EuropeEURORDIS The international voice of people living with rare diseasesRare Disease International Bringing together patients, families and experts to share experiences in a moderated multi-language forum. RareConnect The Rare Barometer Programme is a EURORDIS initiative that carries out surveys to transform rare disease patients' experiences into figures and facts that can be shared with decision-makers.Rare Barometer An international awareness raising campaign taking place on the last day of February each year, Rare Disease Day is a EURORDIS initiativeRare Disease Day Join the largest gathering of rare disease stakeholders across Europe, at the biennial European Conference on Rare Diseases and Orphan Products. ECRD is a EURORDIS initiativeEuropean Conference on Rare Diseases