1. Regulation (EC) No 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) No 726/2004
2. Guideline on human cell-based medicinal products (EMEA/CHMP/410869/2006) of the European Medicines Agency
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
4. Directive 2004/9/EC of The European Parliament and of The Council of 11 February 2004 on the inspection and verification of good laboratory practice (GLP)
5. Directive 2004/10/EC of the European Parliament and of The Council of 11 February 2004 on the harmonisation of laws, regulations and administrative provisions relating to the application of the principles of good laboratory practice and the verification of their applications for tests on chemical substances