Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Text with EEA relevance)
Modified by
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
July 2, 2012 article 18 Replacement
July 2, 2012 article 64 2 Replacement
July 2, 2012 article 57 Replacement
July 2, 2012 article 87 Addition
July 2, 2012 article 14 Replacement
July 2, 2012 article 9 4 Addition
July 2, 2012 article 10 Replacement
July 2, 2012 article 19 Replacement
July 2, 2012 article 16 Replacement
July 2, 2012 article 56 1 Replacement
July 2, 2012 article 10 1 Replacement
July 2, 2012 article 62 Replacement
July 2, 2012 chapter III 2 Replacement
July 2, 2012 article 83 6.2 Replacement
July 2, 2012 article 5 2 Addition
July 2, 2012 article 67 Replacement
July 2, 2012 article 10 TER Addition
July 2, 2012 article 10 6 Replacement
July 2, 2012 article 66 G Replacement
July 2, 2012 article 10 BIS Addition
July 2, 2012 article 20 Replacement
July 2, 2012 article 82 3 Replacement