A Review of Rare Disease Policies and Orphan Drug Reimbursement Systems in 12 Eurasian Countries

A Review of Rare Disease Policies and Orphan Drug Reimbursement Systems in 12 Eurasian Countries

Background: Despite international initiatives on collaboration within the field of rare diseases, patient access to orphan medicinal products (OMPs) and healthcare services differ greatly between countries. This study aimed to create a comprehensive and in-depth overview of rare diseases policies an...

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Bibliographic Details
Main Authors: Marcin Czech, Aleksandra Baran-Kooiker, Kagan Atikeler, Maria Demirtshyan, Kamilla Gaitova, Malwina Holownia-Voloskova, Adina Turcu-Stiolica, Coen Kooiker, Oresta Piniazhko, Natella Konstandyan, Olha Zalis'ka, Jolanta Sykut-Cegielska
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-01-01
Series:Frontiers in Public Health
Subjects:
rare diseases
newborn screening
national plan
patient registries
reimbursement
policy
Online Access:https://www.frontiersin.org/article/10.3389/fpubh.2019.00416/full

Internet

https://www.frontiersin.org/article/10.3389/fpubh.2019.00416/full

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