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2. Regulation (EC) No 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products (ATMPs) and amending Directive 2001/83/EC and Regulation (EC) No 726/2004 (Status as of July 25th 2019).
3. EudraLex: the rules governing medicinal products in the European Union Volume 4: good manufacturing practice: guidelines on good manufacturing practice specific to advanced therapy medicinal products (Status as of November 22nd 2017).
4. Regulation (EC) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC (Status as of May 27th 2014).
5. Directive 2004/23/EC of the European Parliament and of the Council of March 31st 2004 on setting standards of quality and safety for the donation, procurement, testing, processing, preservation, storage and distribution of human tissues and cells (Status as of August 8th 2009).