1. Clinical evaluation of medical devices: light at the end of the tunnel?;Fraser;Eur Heart J,2015
2. Council Directive 93/42/EEC of 14 June 1993 concerning medical devices. http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=CONSLEG:1993L0042:20071011:en:PDF (26 May 2015).
3. Directive 2007/47/EC of the European Parliament and of the council of 5 September 2007 amending council directive 90/385/EEC on the approximation of the laws of the member states relating to active implantable medical devices, council directive 93/42/EEC concerning medical devices and directive 98/8/EC concerning the placing of biocidal products on the market, 2007. http://ec.europa.eu/health/medical-devices/files/revision_docs/2007-47-en_en.pdf (26 May 2015).
4. Clinical evaluation of cardiovascular devices: principles, problems, and proposals for European regulatory reform: Report of a policy conference of the European Society of Cardiology
5. Committee for Medicinal products for human use (CHMP).Guideline on the clinical and non clinical evaluation during the consultation procedure on medcial substances contained in drug eluting (medical substance-eluting) coronary stents, 2009. http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2009/09/WC500003275.pdf (26 May 15).