Patient access to orphan drugs in France

Author:

Bourdoncle Marion,Juillard-Condat Blandine,Taboulet Florence

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Reference53 articles.

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2. Le Cam Y. Inventory of Access and Prices of orphan drugs across Europe: a collaboration work between national alliances on rare diseases and Eurordis. 2010. https://img2.eurordis.org/newsletter/pdf/mar-2011/ERTC_13122010_YLeCam_Final.pdf . Accessed 07 Sep 2016.

3. Detiček A, Locatelli I, Kos M. Patient Access to Medicines for Rare Diseases in European Countries. Value in Health. 2018. https://www.sciencedirect.com/science/article/pii/S109830151830189X . Accessed 24 March 2018

4. Chaffotec AL. Trajectoires de soins et facteurs sociodémographiques : l’exemple des maladies rares en France, care path and sociodemographic attributes: the case of rare diseases in France. Journal de gestion et d'économie médicales. 2015;32(5):389–409.

5. Gridchyna I, Aulois-Griot M. La rétrocession de médicaments par les hôpitaux : quels bénéfices pour les acteurs ? Médecine Droit. 2011;110:203–10.

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