Leit í EES-gagnagrunni
Commission Decision of 21 November 2008 establishing of a list of herbal substances, preparations and combinations thereof for use in traditional herbal medicinal products (notified under document number C(2008) 6933)
Ákvörðun framkvæmdastjórnarinnar frá 21. nóvember 2008 um að taka saman skrá yfir jurtaefni, fullbúin jurtalyf og samsetningar þeirra til notkunar í jurtalyf sem hefð er fyrir (2008/911/EB)
Commission Regulation (EC) No 1234/2008 of 24 November 2008 concerning the examination of variations to the terms of marketing authorisations for medicinal products for human use and veterinary medicinal products
Reglugerð framkvæmdastjórnarinnar (EB) nr. 1234/2008 frá 24. nóvember 2008 um umfjöllun um breytingar á skilmálum markaðsleyfa fyrir mannalyfjum og dýralyfjum
Commission Regulation (EC) No 542/2008 of 16 June 2008 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, as regards cyfluthrin and lectin extracted from red kidney beans (Phaseolus vulgaris)
Commission Regulation (EC) No 203/2008 of 4 March 2008 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, as regards gamithromycin
Commission Regulation (EC) No 61/2008 of 24 January 2008 amending Annex 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, as regards dinoprostone
Reglugerð framkvæmdastjórnarinnar (EB) nr. 61/2008 frá 24. janúar 2008 um breytingu á II. 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 að því er varðar dínóprostón
Regulation (EC) No 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) No 726/2004
Reglugerð Evrópuþingsins og ráðsins (EB) nr. 1394/2007 frá 13. nóvember 2007 um hátæknimeðferðarlyf og breytingu á tilskipun 2001/83/EB og reglugerð (EB) nr. 726/2004
Commission Regulation (EC) No 1353/2007 of 20 November 2007 amending Annex I 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, as regards Monensin, Lasalocid and Tylvalosin
Commission Regulation (EC) No 1323/2007 of 12 November 2007 amending Annex I to Council Regulation (EC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin, as regards firocoxib
Commission Regulation (EC) No 1064/2007 of 17 September 2007 amending Annex I 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, as regards Avilamycin
Commission Regulation (EC) No 703/2007 of 21 June 2007 amending Annex I 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, as regards Dihydrostreptomycin and Streptomycin
Reglugerð framkvæmdastjórnarinnar (EB) nr. 703/2007 frá 21. júní 2007 um breytingu á I. 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 að því er varðar tvívetnisstreptómýsín og streptómýsín
Commission Regulation (EC) No 658/2007 of 14 June 2007 concerning financial penalties for infringement of certain obligations in connection with marketing authorisations granted under Regulation (EC) No 726/2004 of the European Parliament and of the Council
Reglugerð framkvæmdastjórnarinnar (EB) nr. 658/2007 frá 14. júní 2007 um fjárhagsleg viðurlög við brotum á tilteknum skyldum í tengslum við markaðsleyfi sem veitt eru samkvæmt reglugerð Evrópuþingsins og ráðsins (EB) nr. 726/2004
Commission Regulation (EC) No 287/2007 of 16 March 2007 amending Annex 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, as regards Ginseng, standardised extracts and preparations thereof
Reglugerð framkvæmdastjórnarinnar (EB) nr. 287/2007 frá 16. mars 2007 um breytingu, að því er varðar ginseng, stöðluð útdráttarefni úr því og blöndur, á II. 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
Regulation (EC) No 1901/2006 of the European Parliament and of the Council of 12 December 2006 on medicinal products for paediatric use and amending Regulation (EEC) No 1768/92, Directive 2001/20/EC, Directive 2001/83/EC and Regulation (EC) No 726/2004
Reglugerð Evrópuþingsins og ráðsins (EB) nr. 1901/2006 frá 12. desember 2006 um lyf fyrir börn og um breytingu á reglugerð (EBE) nr. 1768/92, tilskipun 2001/20/EB, tilskipun 2001/83/EB og reglugerð (EB) nr. 726/2004