D045785/02
Commission Implementing Decision (EU) 2016/1365 of 9 August 2016 amending Decision 98/536/EC as regards the list of national reference laboratories
Framkvæmdarákvörðun framkvæmdastjórnarinnar (ESB) 2016/1365 frá 9. ágúst 2016 um breytingu á ákvörðun 98/536/EB að því er varðar skrána yfir landsbundnar tilvísuna r rannsóknarstofur
Commission Implementing Decision (EU) 2015/2444 of 17 December 2015 laying down standard requirements for the submission by Member States of national programmes for the eradication, control and surveillance of animal diseases and zoonoses for Union financing and repealing Decision 2008/425/EC
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
D043379/02
Commission Implementing Decision (EU) 2015/2460 of 23 December 2015 concerning certain protective measures in relation to highly pathogenic avian influenza of subtype H5 in France
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
Commission Implementing Decision (EU) 2015/2311 of 9 December 2015 amending Implementing Decisions (EU) 2015/1500 and (EU) 2015/2055 on protective measures against lumpy skin disease in Greece
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
87/448/EEC: Commission Decision of 31 July 1987 authorizing the United Kingdom to restrict the marketing of seed of a variety of an agricultural plant species (Only the English text is authentic)
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
80/128/EEC: Commission Decision of 28 December 1979 authorizing the United Kingdom to restrict the marketing of seed of certain varieties of agricultural plant species (Only the English text is authentic)
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
87/309/EEC: Commission Decision of 2 June 1987 authorizing the indelible printing of prescribed information on packages of seed of certain fodder plant species
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
Commission Implementing Decision (EU) 2015/2291 of 7 December 2015 amending Implementing Decision 2013/722/EU as regards the maximum amount of the Union financial contribution for the programme for the eradication of rabies in Latvia in the year 2014
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
Commission Directive 87/481/EEC of 9 September 1987 amending Council Directive 70/458/EEC on the marketing of vegetable seed
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
Council Directive 79/967/EEC of 12 November 1979 amending Directives 66/403/EEC, 70/457/EEC and 70/458/EEC on the marketing of seed potatoes, the common catalogue of varieties of agricultural plant species and the marketing of vegetable seed
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
D042408/03
Commission Implementing Decision (EU) 2015/2433 of 18 December 2015 amending Implementing Decision 2014/709/EU as regards the animal health control measures relating to African swine fever in certain Member States
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
Commission Implementing Decision (EU) 2015/2239 of 2 December 2015 concerning certain protective measures in relation to highly pathogenic avian influenza of subtypes H5N1 and H5N2 in France
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
Council Directive 87/519/EEC of 19 October 1987 amending Directive 74/63/EEC on undesirable substances and products in animal nutrition
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
Commission Directive 87/238/EEC of 1 April 1987 amending the Annexes to Council Directive 74/63/EEC on undesirable substances and products in animal nutrition
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
Commission Directive 87/234/EEC of 31 March 1987 amending the Annex to Council Directive 77/101/EEC on the marketing of straight feedingstuffs
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
First Commission Directive 79/797/EEC of 10 August 1979 amending the Annex to Council Directive 77/101/EEC on the marketing of straight feedingstuffs
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
Council Directive 79/372/EEC of 2 April 1979 amending Directive 77/101/EEC on the marketing of straight feedingstuffs
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
79/837/EEC: Commission Decision of 25 September 1979 laying down the methods of control for maintaining the officially brucellosis-free status of bovine herds in Denmark (Only the Danish text is authentic)
Verði gerð tekin upp í EES-samninginn birtist hún hér á íslensku eftir birtingu í EES-viðbæti
D041108/03
Commission Implementing Regulation (EU) 2015/2306 of 10 December 2015 concerning the authorisation of L-cysteine hydrochloride monohydrate as a feed additive for cats and dogs
Framkvæmdarreglugerð framkvæmdastjórnarinnar (ESB) 2015/2306 frá 10. desember 2015 um leyfi fyrir L-systeínhýdróklóríðmónóhýdratí sem fóðuraukefni fyrir ketti og hunda
D042203/02
Commission Implementing Regulation (EU) 2015/2305 of 10 December 2015 concerning the authorisation of a preparation of endo-1,4-beta-glucanase (EC 3.2.1.4) produced by Trichoderma citrinoviride Bisset (IM SD142) as a feed additive for chickens for fattening, minor poultry species for fattening and weaned piglets, and amending Regulations (EC) No 2148/2004 and (EC) No 1520/2007 (holder of authorisation Huvepharma NV)
Framkvæmdarreglugerð framkvæmdastjórnarinnar (ESB) 2015/2305 frá 10. desember 2015 um leyfi fyrir blöndu með endó-1,4-betaglúkanasa (ECC 3.2.1.4), sem er framleiddur með Trichoderma citrinoviride Bisset (IM SD142), sem fóðuraukefni fyrir eldiskjúklinga, aukategundir alifugla til eldis og fráfærugrísi og um breytingu á reglugerðum (EB) nr. 2148/2004 og (EB) nr. 1520/2007 (leyfishafi er Huvepharma NV)