References
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- 2. IMPACT International Medical Products Anti-counterfeiting Taskforce. The Handbook. Facts, Activities, Documents Developed by the Assembly and the Working Groups, 2006-2010 (2011; 164 pages) http://apps.who.int/medicinedocs/en/m/abstract/Js20967en/.
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- 9. Resolution on Counterfeiting Medicinal Products. European Parliament, September 2006. http://www.europarl.europa.eu/sides/getDoc.do?type=MOTION&reference=B6-2006-0483&language=EN.
- 10. European Parliament. (Brussels 14 May 2007), First European Parliamentary Symposium on Pharmaceuticals, Putting an End to Drug Counterfeiting. www.epp-ed.eu/Press/peve07/docs/070514programme_pharmaceuticals_en%20.pdf.
- 11. Summary of the Impact Assessment, Commission staff working document: Accompanying document to the Proposal for a Directive of the European Parliament and of the Council amending Directive 2001/83/EC as regards the prevention of the entry into the legal supply chain of medicinal products which are falsified in relation to their identity, history or source. SEC (2008) 2674, Brussels, 10 Dec 2008. https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=celex%3A52014SC0208,.
- 12. Impact Assessment, Commission staff working document: Accompanying document to the Proposal for a Directive of the European Parliament and of the Council amending Directive 2001/83/EC as regards the prevention of the entry into the legal supply chain of medicinal products which are falsified in relation to their identity, history or source. SEC (2008) 2674, Brussels, 10 Dec 2008. https://eur-lex.europa.eu/legal-content/BG/TXT/?uri=CELEX:52016SC0410.
- 13. Directive 2011/62/EU of the European Parliament and of the Council of 8 June 2011 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use, as regards the prevention of the entry into the legal supply chain of falsified medicinal products. https://eur-lex.europa.eu/legal-content/en/TXT/?uri=CELEX:32011L0062.
- 14. Commission delegated regulation (EU) 2016/161 of 2 October 2015 supplementing Directive 2001/83/EC of the European Parliament and of the Council by laying down detailed rules for the safety features appearing on the packaging of medicinal products for human use. https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32016R0161].
- 15. National register of BPhU, https://bphu.bg/19_РЕГИСТЪР/22_София-столична.htm?search:13.
- 16. Medicines verification system goes live across EU to better protect patients from falsified medicines, https://www.efpia.eu/news-events/the-efpia-view/statements-press-releases/medicines-verification-system-goes-live-across-eu-to-better-protect-patients-from-falsified-medicines/.
- 17. Official start of Bulgarian medicines verification system, https://www.bgmvo.org/en/single-new/51/.