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Directive[removed]EU of the European Parliament and of the Council of 8 June 2011 amending Directive[removed]EC on the Community code relating to medicinal products for human use, as regards the prevention of the entry i
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Document Date: 2013-10-09 08:55:47

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City

Lisbon / /

Event

Product Issues / /

IndustryTerm

generic medicinal products / retail sale / supply chain / defective products / law-making / retail supply / manufacturing auth / manufacturing practices / penalties systems / falsified medicinal products / non-prescription medicinal products / manufacturing practice / manufacturing plant / medicinal products / manufacturing authorisation / manufacturing processes / brokered medicinal products / manufacturing auth orisation / Manufacturing authorisation holders / wholesale distributor / information society services / certain medicinal products / manufacturing authorisation holder / case-law / person brokering medicinal products / prescription medicinal products / person exporting medicinal products / illegal medicinal products / medicinal product / transaction medicinal products / manufacturing / supply chains / legal supply chain / appropriate quality systems / legitimate medicinal products / electronic commerce / /

Organization

Court of Justice / Information Society / European Economic and Social Committee / EUROPEAN PARLIAMENT / COUNCIL OF THE EUROPEAN UNION / World Health Organisation / European Medicines Agency / United Nations / Committee of the Regions / European Commission / European Union / Council of Europe / /

Position

Any actor / broker / wholesaler / IMPACT General / Official / EN Official / /

Product

products / /

ProgrammingLanguage

EC / L / /

PublishedMedium

Official Journal of the European Union / the Official Journal / the Official Journal of the European Union / /

SocialTag