Leit í EES-gagnagrunni
Commission Regulation (EC) No 249/2009 of 23 March 2009 amending Council Regulation (EC) No 297/95 as regards the adjustment of the fees of the European Medicines Agency to the inflation rate
Reglugerð framkvæmdastjórnarinnar (EB) nr. 249/2009 frá 23. mars 2009 um breytingu á reglugerð ráðsins (EB) nr. 297/95 að því er varðar aðlögun á gjöldum til Lyfjastofnunar Evrópu með tilliti til verðbólgu
Commission Regulation (EC) No 2701/94 of 7 November 1994 amending Annexes I, II, III and IV to Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin
Reglugerð framkvæmdastjórnarinnar (EB) nr. 2701/94 frá 7. nóvember 1994 um breytingu á I., II., III. og IV. viðauka við reglugerð ráðsins (EBE) nr. 2377/90 þar sem mælt er fyrir um sameiginlega aðferð til að ákvarða hámarksmagn leifa dýralyfja í matvælum úr dýraríkinu
Commission Regulation (EC) No 1430/94 of 22 June 1994 amending Annexes I, II, III and IV of Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin
Reglugerð framkvæmdastjórnarinnar (EB) nr. 1430/94 frá 22. júní 1994 um breytingu á I., II., III. og IV. viðauka reglugerðar ráðsins (EBE) nr. 2377/90 þar sem mælt er fyrir um sameiginlega aðferð til að ákvarða hámarksmagn leifa dýralyfja í matvælum úr dýraríkinu
Commission Regulation (EC) No 955/94 of 28 April 1994 amending Annexes I and II of Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin
Reglugerð framkvæmdastjórnarinnar (EBE) nr. 955/94 frá 28. apríl 1994 um breytingu á I. Og II. viðauka reglugerðar ráðsins 2377/90 þar sem mælt er fyrir um sameiginlega aðferð til að ákvarða hámarksmagn leifa dýralyfja í matvælum úr dýraríkinu
Commission Directive 93/46/EEC of 22 June 1993 replacing and modifying the Annexes to Council Directive 92/109/EEC on the manufacture and placing on the market of certain substances used in the illicit manufacture of narcotic drugs and psychotropic substances
Council Directive 92/109/EEC of 14 December 1992 on the manufacture and the placing on the market of certain substances used in the illicit manufacture of narcotic drugs and psychotropic substances
Council Directive 92/28/EEC of 31 March 1992 on the advertising of medicinal products for human use
Council Directive 92/27/EEC of 31 March 1992 on the labelling of medicinal products for human use and on package leaflets
Council Directive 92/26/EEC of 31 March 1992 concerning the classification for the supply of medicinal products for human use
Council Directive 92/25/EEC of 31 March 1992 on the wholesale distribution of medicinal products for human use
Commission Directive 91/412/EEC of 23 July 1991 laying down the principles and guidelines of good manufacturing practice for veterinary medicinal products
COMMISSION REGULATION (EC) No 3426/93 of 14 December 1993 amending Annexes III and IV to Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin
COMMISSION REGULATION (EC) No 3425/93 of 14 December 1993 amending Annexes I and II to Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin
COUNCIL REGULATION (EEC) No 2901/93 of 18 October 1993 amending Annexes I, II, III and IV to Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin
Commission Regulation (EEC) No 895/93 of 16 April 1993 amending Annexes I, II and III of Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin
Commission Regulation (EEC) No 3092/92 of 27 October 1992 amending Annex III to Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin
Commission Regulation (EEC) No 762/92 of 27 March 1992 modifying Annex V to Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin
Commission Regulation (EEC) No 675/92 of 18 March 1992 amending Annexes I and III of Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin
Commission Directive 92/18/EEC of 20 March 1992 modifying the Annex to Council Directive 81/852/EEC on the approximation of the laws of Member States relating to analytical, pharmacotoxicological and clinical standards and protocols in respect of the texting of veterinary medicinal products
Council Directive 92/74/EEC of 22 September 1992 widening the scope of Directive 81/851/EEC on the approximation of provisions laid down by Law, Regulation or Administrative Action relating to veterinary medicinal products and laying down additional provisions on homeopathic veterinary medicinal products
Commission Directive 91/507/EEC of 19 July 1991 modifying the Annex to Council Directive 75/318/EEC on the approximation of the laws of Member States relating to analytical, pharmacotoxicological and clinical standards and protocols in respect of the testing of medicinal products
Council Directive 92/73/EEC of 22 September 1992 widening the scope of Directives 65/65/EEC and 75/319/EEC on the approximation of provisions laid down by Law, Regulation or Administrative Action relating to medicinal products and laying down additional provisions on homeopathic medicinal products
Commission Directive 2009/9/EC of 10 February 2009 amending Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to medicinal products for veterinary use
Tilskipun framkvæmdastjórnarinnar 2009/9/EB frá 10. febrúar 2009 um breytingu á tilskipun Evrópuþingsins og ráðsins 2001/82/EB um Bandalagsreglur um dýralyf
Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL amending, as regards information to the general public on medicinal products for human use subject to medical prescription, 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
Proposal for a DIRECTIVE OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL amending, as regards information to the general public on medicinal products subject to medical prescription, Directive 2001/83/EC on the Community code relating to medicinal products for human use