1. European Regulatory Tools for Advanced Therapy Medicinal Products;Flory;Transfus Med Hemotherapy,2013
2. Regulation (EC) N° 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) N° 726/2004. (https://eur-lex.europa.eu/homepage.html
3. Directive 2001/83/EC of the European Parliament and of the council of 6 November 2001 on the Community code relating to medicinal products for human use. (https://eur-lex.europa.eu/homepage.html
4. Directive 2004/23/EC of the European Parliament and of the Council of 31 March 2004 on setting standards of quality and safety for the donation, procurement, testing, processing, preservation, storage and distribution of human tissues and cells. (https://eur-lex.europa.eu/homepage. html
5. Médicaments de thérapie innovante, Médicaments de thérapie innovante préparé ponctuellement et préparations : Synthèse du cadre réglementaire applicable pour la fabrication, le développement et la mise sur le marché de ces produits. Version 1 du 30 mars 2012. Mise à jour 5 juin 2012. (http://ansm.sante.fr/