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

• প্রধান লেখক: Marcin Czech (লেখক), Aleksandra Baran-Kooiker (লেখক), Kagan Atikeler (লেখক), Maria Demirtshyan (লেখক), Kamilla Gaitova (লেখক), Malwina Holownia-Voloskova (লেখক), Adina Turcu-Stiolica (লেখক), Coen Kooiker (লেখক), Oresta Piniazhko (লেখক), Natella Konstandyan (লেখক), Olha Zalis'ka (লেখক), Jolanta Sykut-Cegielska (লেখক)
• বিন্যাস: গ্রন্থ
• প্রকাশিত: Frontiers Media S.A., 2020-01-01T00:00:00Z.
• বিষয়গুলি: article
• অনলাইন ব্যবহার করুন: Connect to this object online.

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...