Европейската комисия информира, че през 2025 г. ще бъде обявена нова покана за включване на нови асоциирани партньори в Европейските референтни мрежи за редки заболявания, като процедурата трабва да е финализирана до 2026 г.
Европейски референтни мрежи
На 15 декември 2016 г. Бордът на страните членки на ЕС за европейските референтни мрежи одобри 23 мрежи. 7 Експертни центъра по редки болести от България са одобрени за участие в 5 от тези мрежи – ERN EuroBloodNet (2 центъра), ERN EURO-NMD (1 център), Endo-ERN (2 центъра), MetabERN (1 център) и ERN RND (1 център).
Пълният списък на одобрените референтни мрежи е достъпен на сайта на Европейската комисия: http://ec.europa.eu/health/ern/
The Commission for Rare Diseases was established by Order of the Minister of Health. By Order №16 from 30.07.2014, the Ministry of Health are certain terms and conditions for registration of rare diseases and centers of expertise and reference networks for rare diseases. / the word "Ordinance 16" is a link to the ordinance itself /. The administrative and technical servicing of the commission's activity is provided by the National Center for Public Health and Analysis. The Commission assists the Minister of Health and the Director of the National Center for Public Health and Analysis by:
Register of expert centers for rare diseases in Bulgaria
Application for a disease proposal for inclusion in the List of Rare Diseases
Application for a designation of an expert center for a rare disease / rare diseases
Order of the Ministry of Health to supplement the List of Rare Diseases - 27.02.2020
Order of the Ministry of Health to supplement the List of Rare Diseases - 10.01.2019
Order of the Ministry of Health to supplement the List of Rare Diseases - 04.04.2017
Order of the Ministry of Health to supplement the List of Rare Diseases - 30.03.2016
Order of the Ministry of Health for approval of the List of rare diseases - 27.11.2015
Disease records included in the List of Rare Diseases
European portal for rare diseases Orphanet
Genetic and Rare Diseases Information Center, National Institutes of Health, USA
Information center for rare diseases and orphan drugs
Directorate-General for Health and Food Safety (SANTE), European Commission