Animal Remedies. Animal Remedies Act 1993 (other than sections 4 and 5) Act No. 23 of 1993 European Communities (Control of Animal Remedies and their Residues) Regulations, 2009 (excluding Regulations 3,8,9-12, 16, 20 and 26) S.I. No. 183 of 2009 S.I. No. 263 of 2012 Commission Regulation (EC) No 124/2009 of 10 February 2009 setting maximum levels for the presence of coccidiostats or histomonostats in food resulting from the unavoidable carry-over of these substances in non-target feed. Commission Regulation (EC) No. 124/2009 Commission Implementing Regulation (EU) No. 436/2012 of 23 May 2012 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance azamethiphos. Commission Implementing Regulation (EU) No. 466/2012 of 1 June 2012 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically Commission Implementing Regulation (EU) No. 436/2012 Commission Implementing Regulation (EU) No. 466/2012 active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance clorsulon. Commission Implementing Regulation (EU) No. 1161/2012 of 7 December 2012 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance fenbendazole. Commission Implementing Regulation (EU) No. 1186/2012 of 11 December 2012 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance phoxim. Commission Implementing Regulation (EU) No. 1191/2012 of 12 December 2012 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance sodium salicylate. Commission Implementing Regulation (EU) No. 59/2013 of 23 January 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance monensin. Commission Implementing Regulation (EU) No. 115/2013 of 8 February 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance diclazuril. Commission Implementing Regulation (EU) No. 116/2013 of 8 February 2013 amending the Annex to Regulation (EU) No. 37/2010 on Commission Implementing Regulation (EU) No. 1161/2012 Commission Implementing Regulation (EU) No. 1186/2012 Commission Implementing Regulation (EU) No. 1191/2012 Commission Implementing Regulation (EU) No. 59/2013 Commission Implementing Regulation (EU) No. 115/2013 Commission Implementing Regulation (EU) No. 116/2013 pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance eprinomectin. Commission Implementing Regulation (EU) No. 394/2013 of 29 April 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance monepantel. Commission Implementing Regulation (EU) No. 406/2013 of 2 May 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance prednisolone. Commission Implementing Regulation (EU) No. 489/2013 of 27 May 2013amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance double stranded ribonucleic acid homologous to viral ribonucleic acid coding for part of the coat protein and part of the intergenic region of the Israel Acute Paralysis Virus. Commission Implementing Regulation (EU) No. 1056/2013 of 29 October 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance neomycin. Commission Implementing Regulation (EU) No. 1057/2013 of 29 October 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance manganese carbonate. Commission Implementing Regulation (EU) No. 394/2013 Commission Implementing Regulation (EU) No. 406/2013 Commission Implementing Regulation (EU) No. 489/2013 Commission Implementing Regulation (EU) No. 1056/2013 Commission Implementing Regulation (EU) No. 1057/2013 Commission Implementing Regulation (EU) No.1235/2013 Commission Implementing Regulation (EU) No. 1235/2013 of 2 December 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance diclazuril. Commission Implementing Regulation (EU) No. 20/2014 of 10 January 2014 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance butafosfan. Commission Implementing Regulation (EU) No. 200/2014 of 3 March 2014 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance triptorelin acetate. Commission Implementing Regulation (EU) No. 201/2014 of 3 March 2014 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance tildipirosin. Commission Implementing Regulation (EU) No. 418/2014 of 24 April 2014 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance ivermectin. Commission Implementing Regulation (EU) No. 676/2014 of 19 June 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘triclabendazole’. Commission Implementing Regulation (EU) No. 677/2014 of 19 June 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘cabergoline’. Commission Implementing Regulation (EU) No. 20/2014 Commission Implementing Regulation (EU) No. 200/2014 Commission Implementing Regulation (EU) No. 201/2014 Commission Implementing Regulation (EU) No. 418/2014 Commission Implementing Regulation (EU) No. 676/2014 Commission Implementing Regulation (EU) No. 677/2014 Commission Implementing Regulation (EU) No. 681/2014 Commission Implementing Regulation (EU) No. 682/2014 Commission Implementing Regulation (EU) No. 681/2014 of 20 June 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘rafoxanide’. Commission Implementing Regulation (EU) No. 682/2014 of 20 June 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘closantel’. Commission Implementing Regulation (EU) No. 683/2014 of 20 June 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘clorsulon’. Commission Implementing Regulation (EU) No. 967/2014 of 12 September 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘lufenuron’. Commission Implementing Regulation (EU) No. 1277/2014 of 1 December 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘lasalocid’. Commission Implementing Regulation (EU) No. 1359/2014 of 18 December 2014 amending the Annex to Regulation (EU) No. 37/2010, as regards the substance tulathromycin. Commission Implementing Regulation (EU) No. 1390/2014 of 19 December 2014 amending the Annex to Regulation (EU) No. 37/2010, as regards the substance ‘eprinomectin’. Commission Implementing Regulation (EU) 2015/149 of 30 January 2015 amending the Annex to Regulation (EU) No. 37/2010 as regards the substance ‘methylprednisolone’. Commission Implementing Regulation (EU) 2015/150 of 30 January 2015 amending the Annex to Regulation (EU) No. 37/2010 as regards the substance ‘gamithromycin’. Commission Implementing Regulation (EU) No. 683/2014 Commission Implementing Regulation (EU) No. 967/2014 Commission Implementing Regulation (EU) No. 1277/2014 Commission Implementing Regulation (EU) No. 1359/2014 Commission Implementing Regulation (EU) No. 1390/2014 Commission Implementing Regulation (EU) No. 2015/149 Commission Implementing Regulation (EU) No. 2015/150 Commission Implementing Regulation (EU) No. 2015/151 Commission Implementing Regulation (EU) No. 2015/152 Commission Implementing Regulation (EU) No. 2015/394 Commission Implementing Regulation (EU) 2015/151 of 30 January 2015 amending the Annex to Regulation (EU) No. 37/2010 as regards the substance ‘doxycycline’. Commission Implementing Regulation (EU) 2015/152 of 30 January 2015 amending the Annex to Regulation (EU) No. 37/2010, as regards the substance ‘tulathromycin’. Commission Implementing Regulation (EU) 2015/394 of 10 March 2015 amending the Annex to Regulation (EU) No. 37/2010 as regards the substance ‘tulathromycin’. Commission Implementing Regulation (EU) 2015/446 of 17 March 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘barium selenate’. Commission Implementing Regulation (EU) 2015/1078 of 3 July 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘clodronic acid (in the form of disodium salt)’. Commission Implementing Regulation (EU) 2015/1079 of 3 July 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘hexaflumuron’. Commission Implementing Regulation (EU) 2015/1080 of 3 July 2015 amending Regulation (EU) No. 37/2010 as regards the substance 'propyl 4- hydroxybenzoate and its sodium salt'. Commission Implementing Regulation (EU) 2015/1308 of 29 July 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘aluminium salicylate, basic’. Commission Implementing Regulation (EU) 2015/1491 of 3 September 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘virginiamycin’. Commission Implementing Regulation (EU) No. 2015/446 Commission Implementing Regulation (EU) No. 2015/1078 Commission Implementing Regulation (EU) No. 2015/1079 Commission Implementing Regulation (EU) No. 2015/1080 Commission Implementing Regulation (EU) No. 2015/1308 Commission Implementing Regulation (EU) No. 2015/1491 Commission Implementing Regulation (EU) No. 2015/1492 Commission Implementing Regulation (EU) No. 2015/1820 Commission Implementing Regulation (EU) No. 2015/2062 Commission Implementing Regulation (EU) 2015/1492 of 3 September 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘tylvalosin’. Commission Implementing Regulation (EU) 2015/1820 of 9 October 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘Diethylene glycol monoethyl ether.’ Commission Implementing Regulation (EU) 2015/2062 of 17 November 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘sisapronil’. Commission Implementing Regulation (EU) 2016/129 of 1 February 2016 amending Regulation (EU) No. 37/2010 as regards the substance ‘Purified semisolid extract from Humulus lupulus L. containing approximately 48 % of beta acids (as potassium salts). Commission Implementing Regulation (EU) 2016/305 of 3 March 2016 amending Regulation (EU) No. 37/2010 as regards the substance ‘gentamicin’. Commission Implementing Regulation (EU) 2016/312 of 4 March 2016 correcting Regulation (EU) No. 37/2010 as regards the substance ‘tylvalosin’. Commission Implementing Regulation (EU) 2016/576 of 14 April 2016 amending Regulation (EU) No. 37/2010 as regards the substance ‘rafoxanide’. Commission Implementing Regulation (EU) 2016/710 of 12 May 2016 amending Regulation (EU) No. 37/2010 as regards the substance ‘copper carbonate’. Commission Implementing Regulation (EU) 2016/885 of 3 June 2016 amending Regulation (EU) Commission Implementing Regulation (EU) No. 2016/129 Commission Implementing Regulation (EU) No. 2016/305 Commission Implementing Regulation (EU) No. 2016/312 Commission Implementing Regulation (EU) No. 2016/576 Commission Implementing Regulation (EU) No. 2016/710 Commission Implementing Regulation (EU) No. 2016/885 Commission Implementing Regulation (EU) No. 2016/1444 Commission Implementing Regulation (EU) No. 2016/2045 Commission Implementing Regulation (EU) No.2016/2074 Commission Implementing Regulation (EU) 2017/201 No. 37/2010 as regards the substance ‘eprinomectin’. Commission Implementing Regulation (EU) 2016/1444 of 31 August 2016 amending Regulation (EU) No. 37/2010 as regards the substance hydrocortisone aceponate. Commission Implementing Regulation (EU) 2016/2045 of 23 November 2016 amending Regulation (EU) No. 37/2010 as regards the substance gamithromycin. Commission Implementing Regulation (EU) 2016/2074 of 25 November 2016 amending Regulation (EU) No. 37/2010 as regards the substance aluminium salicylate, basic. Commission Implementing Regulation (EU) 2017/201 of 6 February 2017 amending Regulation (EU) No. 37/2010 to classify the substance fluralaner as regards its maximum residue limit. Commission Implementing Regulation (EU) 2017/1558 of 14 September 2017 amending Regulation (EU) No. 37/2010 to classify the substance bromelain as regards its maximum residue limit. Commission Implementing Regulation (EU) 2017/1559 of 14 September 2017 amending Regulation (EU) No. 37/2010 to classify the maximum residue limit of the substance alarelin. Commission Implementing Regulation (EU) 2018/520 of 28 March 2018 amending Regulation (EU) No. 37/2010 to classify the substance solvent naphtha, light aromatic, as regards its maximum residue limit. Commission Implementing Regulation (EU) 2018/523 of 28 March 2018 amending Regulation (EU) No. 37/2010 to classify the substance fluazuron as regards its maximum residue limit. Commission Implementing Regulation (EU) No. 2017/1558 Commission Implementing Regulation (EU) No. 2017/1559 Commission Implementing Regulation (EU) No. 2018/520 Commission Implementing Regulation (EU) No. 2018/523 Commission Implementing Regulation (EU) No. 2018/721 Commission Implementing Regulation (EU) No. 2018/722 Commission Implementing Regulation (EU) No. 2018/1076 Commission Implementing Regulation (EU) 2018/721 of 16 May 2018 amending Regulation (EU) No. 37/2010 to classify the substance porcine prolactin as regards its maximum residue limit. Commission Implementing Regulation (EU) 2018/722 of 16 May 2018 amending Regulation (EU) No. 37/2010 to classify the substance eprinomectin as regards its maximum residue limit. Commission Implementing Regulation (EU) 2018/1076 of 30 July 2018 amending Regulation (EU) No. 37/2010 to classify the substance isoflurane as regards its maximum residue limit.
Appears in 4 contracts
Samples: www.fsai.ie, www.fsai.ie, www.fsai.ie
Animal Remedies. Animal Remedies Act Act, 1993 (other than sections 4 and 5) Act No. 23 of 1993 European Communities (Control of Animal Remedies and their Residues) Regulations, 2009 (excluding Regulations 3,8,9-12, 16, 20 and 26) S.I. No. 183 of 2009 S.I. No. 263 of 2012 Commission Regulation (EC) No 124/2009 of 10 February 2009 setting maximum levels for the presence of coccidiostats or histomonostats in food resulting from the unavoidable carry-over of these substances in non-target feed. Commission Regulation (EC) No. 124/2009 Commission Implementing Regulation (EU) No. 436/2012 of 23 May 2012 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance azamethiphos. Commission Implementing Regulation (EU) No. 466/2012 of 1 June 2012 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically Commission Implementing Regulation (EU) No. 436/2012 Commission Implementing Regulation (EU) No. 466/2012 active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance clorsulon. Commission Implementing Regulation (EU) No. 1161/2012 of 7 December 2012 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance fenbendazole. Commission Implementing Regulation (EU) No. 1186/2012 of 11 December 2012 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance phoxim. Commission Implementing Regulation (EU) No. 1191/2012 of 12 December 2012 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance sodium salicylate. Commission Implementing Regulation (EU) No. 436/2012 Commission Implementing Regulation (EU) No. 466/2012 Commission Implementing Regulation (EU) No. 1161/2012 Commission Implementing Regulation (EU) No. 1186/2012 Commission Implementing Regulation (EU) No. 1191/2012 Commission Implementing Regulation (EU) No. 59/2013 of 23 January 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance monensin. Commission Implementing Regulation (EU) No. 115/2013 of 8 February 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance diclazuril. Commission Implementing Regulation (EU) No. 116/2013 of 8 February 2013 amending the Annex to Regulation (EU) No. 37/2010 on Commission Implementing Regulation (EU) No. 1161/2012 Commission Implementing Regulation (EU) No. 1186/2012 Commission Implementing Regulation (EU) No. 1191/2012 Commission Implementing Regulation (EU) No. 59/2013 Commission Implementing Regulation (EU) No. 115/2013 Commission Implementing Regulation (EU) No. 116/2013 pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance eprinomectin. Commission Implementing Regulation (EU) No. 394/2013 of 29 April 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance monepantel. Commission Implementing Regulation (EU) No. 406/2013 of 2 May 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance prednisolone. Commission Implementing Regulation (EU) No. 489/2013 of 27 May 2013amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance double stranded ribonucleic acid homologous to viral ribonucleic acid coding for part of the coat protein and part of the intergenic region of the Israel Acute Paralysis Virus. Commission Implementing Regulation (EU) No. Commission Implementing Regulation (EU) No. 59/2013 Commission Implementing Regulation (EU) No. 115/2013 Commission Implementing Regulation (EU) No. 116/2013 Commission Implementing Regulation (EU) No. 394/2013 Commission Implementing Regulation (EU) No. 406/2013 Commission Implementing Regulation (EU) No. 489/2013 Commission Implementing 1056/2013 of 29 October 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance neomycin. Commission Implementing Regulation (EU) No. 1057/2013 of 29 October 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance manganese carbonate. Commission Implementing Regulation (EU) No. 394/2013 Commission Implementing Regulation (EU) No. 406/2013 Commission Implementing Regulation (EU) No. 489/2013 Commission Implementing Regulation (EU) No. 1056/2013 Commission Implementing Regulation (EU) No. 1057/2013 Commission Implementing Regulation (EU) No.1235/2013 Commission Implementing Regulation (EU) No. 1235/2013 of 2 December 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance diclazuril. Commission Implementing Regulation (EU) No. 20/2014 of 10 January 2014 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance butafosfan. Commission Implementing Regulation (EU) No. 200/2014 of 3 March 2014 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance triptorelin acetate. Commission Implementing Regulation (EU) No. 201/2014 of 3 March 2014 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance tildipirosin. Commission Implementing Regulation (EU) No. 418/2014 of 24 April 2014 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance ivermectin. Regulation (EU) No. 1056/2013 Commission Implementing Regulation (EU) No. 1057/2013 Commission Implementing Regulation (EU) No.1235/2013 Commission Implementing Regulation (EU) No. 20/2014 Commission Implementing Regulation (EU) No. 200/2014 Commission Implementing Regulation (EU) No. 201/2014 Commission Implementing Regulation (EU) No. 418/2014 Commission Implementing Regulation (EU) No. 676/2014 of 19 June 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘triclabendazole’. Commission Implementing Regulation (EU) No. 677/2014 of 19 June 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘cabergoline’. Commission Implementing Regulation (EU) No. 20/2014 Commission Implementing Regulation (EU) No. 200/2014 Commission Implementing Regulation (EU) No. 201/2014 Commission Implementing Regulation (EU) No. 418/2014 Commission Implementing Regulation (EU) No. 676/2014 Commission Implementing Regulation (EU) No. 677/2014 Commission Implementing Regulation (EU) No. 681/2014 Commission Implementing Regulation (EU) No. 682/2014 Commission Implementing Regulation (EU) No. 681/2014 of 20 June 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘rafoxanide’. Commission Implementing Regulation (EU) No. 682/2014 of 20 June 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘closantel’. Commission Implementing Regulation (EU) No. 683/2014 of 20 June 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘clorsulon’. Commission Implementing Regulation (EU) No. 967/2014 of 12 September 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘lufenuron’. Commission Implementing Regulation (EU) No. 1277/2014 of 1 December 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘lasalocid’. Commission Implementing Regulation (EU) No. 1359/2014 of 18 December 2014 amending the Annex to Regulation (EU) No. 37/2010, as regards the substance tulathromycin. Commission Implementing Regulation (EU) No. 1390/2014 of 19 December 2014 amending the Annex to Regulation (EU) No. 37/2010, as regards the substance ‘eprinomectin’. Commission Implementing Regulation (EU) 2015/149 of 30 January 2015 amending the Annex to Regulation (EU) No. 37/2010 as regards the substance ‘methylprednisolone’. Commission Implementing Regulation (EU) 2015/150 of 30 January 2015 amending the Annex to Regulation Commission Implementing Regulation (EU) No. 37/2010 as regards the substance ‘gamithromycin’676/2014 Commission Implementing Regulation (EU) No. 677/2014 Commission Implementing Regulation (EU) No. 681/2014 Commission Implementing Regulation (EU) No. 682/2014 Commission Implementing Regulation (EU) No. 683/2014 Commission Implementing Regulation (EU) No. 967/2014 Commission Implementing Regulation (EU) No. 1277/2014 Commission Implementing Regulation (EU) No. 1359/2014 Commission Implementing Regulation (EU) No. 1390/2014 Commission Implementing Regulation (EU) NoXx. 2015/149 Commission Implementing Regulation 0000/000 Xxxxxxxxxx Xxxxxxxxxxxx Xxxxxxxxxx (EUXX) NoXx. 2015/150 Commission Implementing Regulation (EU) No. 2015/151 Commission Implementing Regulation (EU) No. 2015/152 Commission Implementing Regulation (EU) No. 2015/394 Commission Implementing Regulation (EU) 2015/151 of 30 January 2015 amending the Annex to Regulation (EU) No. 37/2010 as regards the substance ‘doxycycline’. Commission Implementing Regulation (EU) 2015/152 of 30 January 2015 amending the Annex to Regulation (EU) No. 37/2010, as regards the substance ‘tulathromycin’. Commission Implementing Regulation (EU) 2015/394 of 10 March 2015 amending the Annex to Regulation (EU) No. 37/2010 as regards the substance ‘tulathromycin’. Commission Implementing Regulation (EU) 2015/446 of 17 March 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘barium selenate’. Commission Implementing Regulation (EU) 2015/1078 of 3 July 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘clodronic acid (in the form of disodium salt)’. Commission Implementing Regulation (EU) 2015/1079 of 3 July 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘hexaflumuron’. Commission Implementing Regulation (EU) 2015/1080 of 3 July 2015 amending Regulation (EU) No. 37/2010 as regards the substance 'propyl 4- hydroxybenzoate and its sodium salt'. Commission Implementing Regulation (EU) 2015/1308 of 29 July 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘aluminium salicylate, basic’. Commission Implementing Regulation (EU) 2015/1491 of 3 September 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘virginiamycin’. Commission Implementing Regulation (EU) No. 2015/446 Commission Implementing Regulation (EU) No. 2015/1078 Commission Implementing Regulation (EU) No. 2015/1079 Commission Implementing Regulation (EU) No. 2015/1080 Commission Implementing Regulation (EU) No. 2015/1308 Commission Implementing Regulation (EU) No. 2015/1491 Commission Implementing Regulation (EU) No. 2015/1492 Commission Implementing Regulation (EU) No. 2015/1820 Commission Implementing Regulation (EU) No. 2015/2062 Commission Implementing Regulation (EU) 2015/1492 of 3 September 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘tylvalosin’. Commission Implementing Regulation (EU) 2015/1820 of 9 October 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘Diethylene glycol monoethyl ether.’ Commission Implementing Regulation (EU) 2015/2062 of 17 November 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘sisapronil’. Commission Implementing Regulation (EU) 2016/129 of 1 February 2016 amending Regulation (EU) No. 37/2010 as regards the substance ‘Purified semisolid extract from Humulus lupulus L. containing approximately 48 % of beta acids (as potassium salts). Commission Implementing Regulation (EU) 2016/305 of 3 March 2016 amending Regulation (EU) No. 37/2010 as regards the substance ‘gentamicin’. Commission Implementing Regulation (EU) 2016/312 of 4 March 2016 correcting Regulation (EU) No. 37/2010 as regards the substance ‘tylvalosin’. Commission Implementing Regulation (EU) 2016/576 of 14 April 2016 amending Regulation (EU) No. 37/2010 as regards the substance ‘rafoxanide’. Commission Implementing Regulation (EU) 2016/710 of 12 May 2016 amending Regulation (EU) No. 37/2010 as regards the substance ‘copper carbonate’. Commission Implementing Regulation (EU) 2016/885 of 3 June 2016 amending Regulation (EU) Commission Implementing Regulation (EU) No. 2016/129 Commission Implementing Regulation (EU) No. 2016/305 Commission Implementing Regulation (EU) No. 2016/312 Commission Implementing Regulation (EU) No. 2016/576 Commission Implementing Regulation (EU) No. 2016/710 Commission Implementing Regulation (EU) No. 2016/885 Commission Implementing Regulation (EU) No. 2016/1444 Commission Implementing Regulation (EU) No. 2016/2045 Commission Implementing Regulation (EU) No.2016/2074 Commission Implementing Regulation (EU) 2017/201 No. 37/2010 as regards the substance ‘eprinomectin’. Commission Implementing Regulation (EU) 2016/1444 of 31 August 2016 amending Regulation (EU) No. 37/2010 as regards the substance hydrocortisone aceponate. Commission Implementing Regulation (EU) 2016/2045 of 23 November 2016 amending Regulation (EU) No. 37/2010 as regards the substance gamithromycin. Commission Implementing Regulation (EU) 2016/2074 of 25 November 2016 amending Regulation (EU) No. 37/2010 as regards the substance aluminium salicylate, basic. Commission Implementing Regulation (EU) 2017/201 of 6 February 2017 amending Regulation (EU) No. 37/2010 to classify the substance fluralaner as regards its maximum residue limit. Commission Implementing Regulation (EU) 2017/1558 of 14 September 2017 amending Regulation (EU) No. 37/2010 to classify the substance bromelain as regards its maximum residue limit. Commission Implementing Regulation (EU) 2017/1559 of 14 September 2017 amending Regulation (EU) No. 37/2010 to classify the maximum residue limit of the substance alarelin. Commission Implementing Regulation (EU) 2018/520 of 28 March 2018 amending Regulation (EU) No. 37/2010 to classify the substance solvent naphtha, light aromatic, as regards its maximum residue limit. Commission Implementing Regulation (EU) 2018/523 of 28 March 2018 amending Regulation (EU) No. 37/2010 to classify the substance fluazuron as regards its maximum residue limit. Commission Implementing Regulation (EU) No. 2017/1558 Commission Implementing Regulation (EU) No. 2017/1559 Commission Implementing Regulation (EU) No. 2018/520 Commission Implementing Regulation (EU) No. 2018/523 Commission Implementing Regulation (EU) No. 2018/721 Commission Implementing Regulation (EU) No. 2018/722 Commission Implementing Regulation (EU) No. 2018/1076 Commission Implementing Regulation (EU) 2018/721 of 16 May 2018 amending Regulation (EU) No. 37/2010 to classify the substance porcine prolactin as regards its maximum residue limit. Commission Implementing Regulation (EU) 2018/722 of 16 May 2018 amending Regulation (EU) No. 37/2010 to classify the substance eprinomectin as regards its maximum residue limit. Commission Implementing Regulation (EU) 2018/1076 of 30 July 2018 amending Regulation (EU) No. 37/2010 to classify the substance isoflurane as regards its maximum residue limit.0000/000
Appears in 1 contract
Samples: www.fsai.ie
Animal Remedies. Animal Remedies Act 1993 (other than sections 4 and 5) Act No. 23 of 1993 European Communities (Control of Animal Remedies and their Residues) Regulations, 2009 (excluding Regulations 3,8,9-12, 16, 20 and 26) S.I. No. 183 of 2009 S.I. No. 263 of 2012 Commission Regulation (EC) No 124/2009 of 10 February 2009 setting maximum levels for the presence of coccidiostats or histomonostats in food resulting from the unavoidable carry-over of these substances in non-target feed. Commission Regulation (EC) No. 124/2009 Commission Implementing Regulation (EU) No. 436/2012 of 23 May 2012 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance azamethiphos. Commission Implementing Regulation (EU) No. 466/2012 of 1 June 2012 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically Commission Implementing Regulation (EU) No. 436/2012 Commission Implementing Regulation (EU) No. 466/2012 active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance clorsulon. Commission Implementing Regulation (EU) No. 1161/2012 of 7 December 2012 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance fenbendazole. Commission Implementing Regulation (EU) No. 1186/2012 of 11 December 2012 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance phoxim. Commission Implementing Regulation (EU) No. 1191/2012 of 12 December 2012 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance sodium salicylate. Commission Implementing Regulation (EU) No. 59/2013 of 23 January 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance monensin. Commission Implementing Regulation (EU) No. 115/2013 of 8 February 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance diclazuril. Commission Implementing Regulation (EU) No. 116/2013 of 8 February 2013 amending the Annex to Regulation (EU) No. 37/2010 on Commission Implementing Regulation (EU) No. 1161/2012 Commission Implementing Regulation (EU) No. 1186/2012 Commission Implementing Regulation (EU) No. 1191/2012 Commission Implementing Regulation (EU) No. 59/2013 Commission Implementing Regulation (EU) No. 115/2013 Commission Implementing Regulation (EU) No. 116/2013 pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance eprinomectin. Commission Implementing Regulation (EU) No. 394/2013 of 29 April 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance monepantel. Commission Implementing Regulation (EU) No. 406/2013 of 2 May 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance prednisolone. Commission Implementing Regulation (EU) No. 489/2013 of 27 May 2013amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance double stranded ribonucleic acid homologous to viral ribonucleic acid coding for part of the coat protein and part of the intergenic region of the Israel Acute Paralysis Virus. Commission Implementing Regulation (EU) No. 1056/2013 of 29 October 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance neomycin. Commission Implementing Regulation (EU) No. 1057/2013 of 29 October 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance manganese carbonate. Commission Implementing Regulation (EU) No. 394/2013 Commission Implementing Regulation (EU) No. 406/2013 Commission Implementing Regulation (EU) No. 489/2013 Commission Implementing Regulation (EU) No. 1056/2013 Commission Implementing Regulation (EU) No. 1057/2013 Commission Implementing Regulation (EU) No.1235/2013 Commission Implementing Regulation (EU) No. 1235/2013 of 2 December 2013 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance diclazuril. Commission Implementing Regulation (EU) No. 20/2014 of 10 January 2014 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance butafosfan. Commission Implementing Regulation (EU) No. 200/2014 of 3 March 2014 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance triptorelin acetate. Commission Implementing Regulation (EU) No. 201/2014 of 3 March 2014 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance tildipirosin. Commission Implementing Regulation (EU) No. 418/2014 of 24 April 2014 amending the Annex to Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance ivermectin. Commission Implementing Regulation (EU) No. 676/2014 of 19 June 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘triclabendazole’. Commission Implementing Regulation (EU) No. 677/2014 of 19 June 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘cabergoline’. Commission Implementing Regulation (EU) No. 20/2014 Commission Implementing Regulation (EU) No. 200/2014 Commission Implementing Regulation (EU) No. 201/2014 Commission Implementing Regulation (EU) No. 418/2014 Commission Implementing Regulation (EU) No. 676/2014 Commission Implementing Regulation (EU) No. 677/2014 Commission Implementing Regulation (EU) No. 681/2014 Commission Implementing Regulation (EU) No. 682/2014 Commission Implementing Regulation (EU) No. 681/2014 of 20 June 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘rafoxanide’. Commission Implementing Regulation (EU) No. 682/2014 of 20 June 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘closantel’. Commission Implementing Regulation (EU) No. 683/2014 of 20 June 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘clorsulon’. Commission Implementing Regulation (EU) No. 967/2014 of 12 September 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘lufenuron’. Commission Implementing Regulation (EU) No. 1277/2014 of 1 December 2014 amending Regulation (EU) No. 37/2010, as regards the substance ‘lasalocid’. Commission Implementing Regulation (EU) No. 1359/2014 of 18 December 2014 amending the Annex to Regulation (EU) No. 37/2010, as regards the substance tulathromycin. Commission Implementing Regulation (EU) No. 1390/2014 of 19 December 2014 amending the Annex to Regulation (EU) No. 37/2010, as regards the substance ‘eprinomectin’. Commission Implementing Regulation (EU) 2015/149 of 30 January 2015 amending the Annex to Regulation (EU) No. 37/2010 as regards the substance ‘methylprednisolone’. Commission Implementing Regulation (EU) 2015/150 of 30 January 2015 amending the Annex to Regulation (EU) No. 37/2010 as regards the substance ‘gamithromycin’. Commission Implementing Regulation (EU) No. 683/2014 Commission Implementing Regulation (EU) No. 967/2014 Commission Implementing Regulation (EU) No. 1277/2014 Commission Implementing Regulation (EU) No. 1359/2014 Commission Implementing Regulation (EU) No. 1390/2014 Commission Implementing Regulation (EU) No. 2015/149 Commission Implementing Regulation (EU) No. 2015/150 Commission Implementing Regulation (EU) No. 2015/151 Commission Implementing Regulation (EU) No. 2015/152 Commission Implementing Regulation (EU) No. 2015/394 Commission Implementing Regulation (EU) 2015/151 of 30 January 2015 amending the Annex to Regulation (EU) No. 37/2010 as regards the substance ‘doxycycline’. Commission Implementing Regulation (EU) 2015/152 of 30 January 2015 amending the Annex to Regulation (EU) No. 37/2010, as regards the substance ‘tulathromycin’. Commission Implementing Regulation (EU) 2015/394 of 10 March 2015 amending the Annex to Regulation (EU) No. 37/2010 as regards the substance ‘tulathromycin’. Commission Implementing Regulation (EU) 2015/446 of 17 March 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘barium selenate’. Commission Implementing Regulation (EU) 2015/1078 of 3 July 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘clodronic acid (in the form of disodium salt)’. Commission Implementing Regulation (EU) 2015/1079 of 3 July 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘hexaflumuron’. Commission Implementing Regulation (EU) 2015/1080 of 3 July 2015 amending Regulation (EU) No. 37/2010 as regards the substance 'propyl 4- hydroxybenzoate and its sodium salt'. Commission Implementing Regulation (EU) 2015/1308 of 29 July 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘aluminium salicylate, basic’. Commission Implementing Regulation (EU) 2015/1491 of 3 September 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘virginiamycin’. Commission Implementing Regulation (EU) No. 2015/446 Commission Implementing Regulation (EU) No. 2015/1078 Commission Implementing Regulation (EU) No. 2015/1079 Commission Implementing Regulation (EU) No. 2015/1080 Commission Implementing Regulation (EU) No. 2015/1308 Commission Implementing Regulation (EU) No. 2015/1491 Commission Implementing Regulation (EU) No. 2015/1492 Commission Implementing Regulation (EU) No. 2015/1820 Commission Implementing Regulation (EU) No. 2015/2062 Commission Implementing Regulation (EU) 2015/1492 of 3 September 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘tylvalosin’. Commission Implementing Regulation (EU) 2015/1820 of 9 October 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘Diethylene glycol monoethyl ether.’ Commission Implementing Regulation (EU) 2015/2062 of 17 November 2015 amending Regulation (EU) No. 37/2010 as regards the substance ‘sisapronil’. Commission Implementing Regulation (EU) 2016/129 of 1 February 2016 amending Regulation (EU) No. 37/2010 as regards the substance ‘Purified semisolid extract from Humulus lupulus L. containing approximately 48 % of beta acids (as potassium salts). Commission Implementing Regulation (EU) 2016/305 of 3 March 2016 amending Regulation (EU) No. 37/2010 as regards the substance ‘gentamicin’. Commission Implementing Regulation (EU) 2016/312 of 4 March 2016 correcting Regulation (EU) No. 37/2010 as regards the substance ‘tylvalosin’. Commission Implementing Regulation (EU) 2016/576 of 14 April 2016 amending Regulation (EU) No. 37/2010 as regards the substance ‘rafoxanide’. Commission Implementing Regulation (EU) 2016/710 of 12 May 2016 amending Regulation (EU) No. 37/2010 as regards the substance ‘copper carbonate’. Commission Implementing Regulation (EU) 2016/885 of 3 June 2016 amending Regulation (EU) Commission Implementing Regulation (EU) No. 2016/129 Commission Implementing Regulation (EU) No. 2016/305 Commission Implementing Regulation (EU) No. 2016/312 Commission Implementing Regulation (EU) No. 2016/576 Commission Implementing Regulation (EU) No. 2016/710 Commission Implementing Regulation (EU) No. 2016/885 Commission Implementing Regulation (EU) No. 2016/1444 Commission Implementing Regulation (EU) No. 2016/2045 Commission Implementing Regulation (EU) No.2016/2074 Commission Implementing Regulation (EU) 2017/201 No. 37/2010 as regards the substance ‘eprinomectin’. Commission Implementing Regulation (EU) 2016/1444 of 31 August 2016 amending Regulation (EU) No. 37/2010 as regards the substance hydrocortisone aceponate. Commission Implementing Regulation (EU) 2016/2045 of 23 November 2016 amending Regulation (EU) No. 37/2010 as regards the substance gamithromycin. Commission Implementing Regulation (EU) 2016/2074 of 25 November 2016 amending Regulation (EU) No. 37/2010 as regards the substance aluminium salicylate, basic. Commission Implementing Regulation (EU) 2017/201 of 6 February 2017 amending Regulation (EU) No. 37/2010 to classify the substance fluralaner as regards its maximum residue limit. Commission Implementing Regulation (EU) 2017/1558 of 14 September 2017 amending Regulation (EU) No. 37/2010 to classify the substance bromelain as regards its maximum residue limit. Commission Implementing Regulation (EU) 2017/1559 of 14 September 2017 amending Regulation (EU) No. 37/2010 to classify the maximum residue limit of the substance alarelin. Commission Implementing Regulation (EU) 2018/520 of 28 March 2018 amending Regulation (EU) No. 37/2010 to classify the substance solvent naphtha, light aromatic, as regards its maximum residue limit. Commission Implementing Regulation (EU) 2018/523 of 28 March 2018 amending Regulation (EU) No. 37/2010 to classify the substance fluazuron as regards its maximum residue limit. Commission Implementing Regulation (EU) No. 2017/1558 Commission Implementing Regulation (EU) No. 2017/1559 Commission Implementing Regulation (EU) No. 2018/520 Commission Implementing Regulation (EU) No. 2018/523 Commission Implementing Regulation (EU) No. 2018/721 Commission Implementing Regulation (EU) No. 2018/722 Commission Implementing Regulation (EU) No. 2018/1076 Commission Implementing Regulation (EU) 2018/721 of 16 May 2018 amending Regulation (EU) No. 37/2010 to classify the substance porcine prolactin as regards its maximum residue limit. Commission Implementing Regulation (EU) 2018/722 of 16 May 2018 amending Regulation (EU) No. 37/2010 to classify the substance eprinomectin as regards its maximum residue limit. Commission Implementing Regulation (EU) 2018/1076 of 30 July 2018 amending Regulation (EU) No. 37/2010 to classify the substance isoflurane as regards its maximum residue limit.
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