Regulation (EU) No 1235/2010 of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance of medicinal products for human use, Regulation (EC) No 726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency, and Regulation (EC) No 1394/2007 on advanced therapy medicinal products Text with EEA relevance
Basic information
Dates Date of document:
  • December 15, 2010
Date of publication:
  • December 31, 2010
Date of effect:
  • January 1, 2011
    • Entry into force - Date pub. +1 See Art 4
  • July 2, 2012
    • Application - See Art 4
Modified by
Corrected by:
Modifies
Modifies:
Affected by case
Legal basis
  • 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)
  • 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)
EuroVoc Vocabulary
  • Veterinary drug
  • Plant health legislation
  • Proprietary medicinal products
  • European Medicines Agency
  • Drug surveillance
  • Public health
  • Marketing
  • Medicinal product
  • Technical barriers