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 Text with EEA relevance
Basic information
Dates Date of document:
  • June 8, 2011
Date of publication:
  • July 1, 2011
Date of effect:
  • July 21, 2011
    • Entry into force - Date pub. +20 See Art 5
Date of transposition:
  • January 2, 2013
    • At the latest See Art 2
Modified by
Modifies
Modifies:
Affected by case
Legal basis
  • Consolidated version of the Treaty on the Functioning of the European Union PART THREE - UNION POLICIES AND INTERNAL ACTIONS TITLE VII - COMMON RULES ON COMPETITION, TAXATION AND APPROXIMATION OF LAWS Chapter 3 - Approximation of laws Article 114(ex Article 95 TEC)
  • Consolidated version of the Treaty on the Functioning of the European Union PART SIX - INSTITUTIONAL AND FINANCIAL PROVISIONS TITLE I - INSTITUTIONAL PROVISIONS Chapter 2 - Legal acts of the Union, adoption procedures and other provisions Section 2 - Procedures for the adoption of acts and other provisions Article 294(ex Article 251 TEC)
  • Consolidated version of the Treaty on the Functioning of the European Union PART THREE - UNION POLICIES AND INTERNAL ACTIONS TITLE XIV - PUBLIC HEALTH Article 168(ex Article 152 TEC)
EuroVoc Vocabulary
  • Medicinal product
  • Market approval
  • Electronic commerce
  • Proprietary medicinal products
  • Industrial counterfeiting
  • Illicit trade
  • Health control
  • Distributive trades
  • Public health