HEALTH POLICIES ABOUT GENE & CELL THERAPIES IN FRANCE, GERMANY, ITALY, UNITED KINGDOM, SPAIN, PORTUGAL AND TURKEY
Öz
Methods: The study followed an inductive research approach with secondary data search which was collected from different online sources to perform areviow on the regulatory process, reimbursement, pricing decisions, and regenerative therapy market.
Results: The United Kingdom, Germany, Italy, Portugal, Spain, and France follow the European Medicines Agency regulatory process for market approval. Turkey does not follow the European Medicines Agency and does not have any defined regulation authority for gene and cell therapy. France, Germany, and the United Kingdom have recently published updated health technology assessment reports. Portugal and Spain do not have nationally approved gene and cell therapy practices, however, have initiated research resource on cellular and gene therapies. The United Kingdom and Germany are the most advanced in the commercialization and legalization of gene and cellular therapies in selected countries.
Conclusion: European countries have variable pricing, reimbursement, and market access regulations apart from the common European Medicines Agency regulations. Improved gene and cell therapy regulations have proven the clinical effectiveness of new treatments. Academic research centers, small and medium businesses are the main components of gene and cell therapy research. The inclusion of gene and cell therapies in guidelines and legislation may improve the market access of these therapies
Anahtar Kelimeler
Kaynakça
- Allied Market Research. (2019). Gene Therapy Market Overview [Fact Sheet]. https://www.alliedmarketresearch.com/gene-therapy- market.
- American Society of Gene & Cell Therapy. (2018). Gene and Cell Therapy [Fact Sheet]. https://www.asgct.org/education/gene-and-cell-therapy- defined.
- APM Health Europe. (2019). https://www.apmhealtheurope.com/index.php
- Blasimme, A., & Rial-Sebbag, E. (2013). “Regulation of cell-based therapies in Europe: current challenges and emerging issues”. Stem cells and development, 22(S1), 14-19.
- Bouslouk, M. (2016). “G-BA benefit assessment of new orphan drugs in Germany: the first five years”. Expert Opin Orphan Drugs, 4(5), 453-455.
- Busse, R., & Blümel, M. (2014). “Germany: health system review”. Health Systems in Transition. https://apps.who.int/iris/bitstream/handle/10665/130246/HiT- 16-2-2014-eng.pdf?sequence=5&isAllowed=y
- Chamova, J., & Stellalliance, A. B. (2017). “Mapping of HTA national organisations, programmes and processes in EU and Norway”. Brussels: European Commission.
- de Wilde, S., Guchelaar, H. J., Herberts, C., Lowdell, M., Hildebrandt, M., Zandvliet, M., & Meij, P. (2016).
Ayrıntılar
Birincil Dil
İngilizce
Konular
Sağlık Kurumları Yönetimi
Bölüm
Derleme
Yazarlar
Güvenç Koçkaya
*
Türkiye
Gulpembe Oguzhan
Türkiye
Furkan Muhammed Ülger
Bu kişi benim
Türkiye
Kardelen Çam
Türkiye
Yayımlanma Tarihi
31 Aralık 2020
Gönderilme Tarihi
18 Kasım 2020
Kabul Tarihi
6 Ocak 2021
Yayımlandığı Sayı
Yıl 2020 Cilt: 4 Sayı: 2