Commission Regulation (EU) No 37/2010 of 22 December 2009 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin (Text with EEA relevance)
Original version: <a href='/vid/commission-regulation-eu-no37-843358182'>Commission Regulation (EU) No 37/2010 of 22 December 2009 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin (Text with EEA relevance)</a>
Linked as:Legal Act History
- Versión futura:
- A partir de 11/06/2023
- Versión actual:
- From
- Versiones pasadas:
- From 09/02/2010 to 25/10/2010
- From 25/10/2010 to 12/12/2010
- From 12/12/2010 to 14/07/2011
- From 14/07/2011 to 09/04/2012
- ↘ More
- From 09/04/2012 to 14/05/2012
- From 14/05/2012 to 01/08/2012
- From 01/08/2012 to 13/02/2013
- From 13/02/2013 to 10/04/2013
- From 10/04/2013 to 03/07/2013
- From 03/07/2013 to 30/12/2013
- From 30/12/2013 to 03/02/2014
- From 03/02/2014 to 24/06/2014
- From 24/06/2014 to 19/08/2014
- From 19/08/2014 to 12/11/2014
- From 12/11/2014 to 22/02/2015
- From 22/02/2015 to 01/04/2015
- From 01/04/2015 to 17/05/2015
- From 17/05/2015 to 02/09/2015
- From 02/09/2015 to 28/09/2015
- From 28/09/2015 to 03/11/2015
- From 03/11/2015 to 09/12/2015
- From 09/12/2015 to 17/01/2016
- From 17/01/2016 to 22/02/2016
- From 22/02/2016 to 24/03/2016
- From 24/03/2016 to 02/06/2016
- From 02/06/2016 to 24/06/2016
- From 24/06/2016 to 31/10/2016
- From 31/10/2016 to 17/12/2016
- From 17/12/2016 to 25/01/2017
- From 25/01/2017 to 08/04/2017
- From 08/04/2017 to 05/10/2017
- From 05/10/2017 to 23/04/2018
- From 23/04/2018 to 03/06/2018
- From 03/06/2018 to 16/07/2018
- From 16/07/2018 to 29/09/2018
- From 29/09/2018 to 11/02/2019
- From 11/02/2019 to 03/03/2019
- From 03/03/2019 to 03/12/2020
- From 03/12/2020 to 06/05/2021
- From 06/05/2021 to 11/06/2023
- ↖ Fewer
Document options
Extract
Commission Regulation (EU) No 37/2010 of 22 December 2009 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin (Text with EEA relevance)
No longer available (Autolink)
See the full content of this document
This document cites
- Minto's Trustees v Minto
- M'Gilp v Caledonian Railway Company
- Dundas v Livingstone & Company
- Christison v Knowles
- Graham v Graham's Trustees
- Company Directors Disqualification Act 1986
- Vehicle Excise and Registration Act 1994
- 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)’ (Text with EEA relevance)
- Commission Implementing Regulation (EU) No 116/2013 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 eprinomectin Text with EEA relevance
- 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 Text with EEA relevance
- Commission Implementing Regulation (EU) No 107/2012 of 8 February 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 octenidine dihydrochloride Text with EEA relevance
- Commission Implementing Regulation (EU) 2015/1492 of 3 September 2015 amending Regulation (EU) No 37/2010 as regards the substance ‘tylvalosin’ (Text with EEA relevance)
- Commission Implementing Regulation (EU) 2015/152 of 30 January 2015 amending the Annex to Regulation (EU) No 37/2010, as regards the substance ‘tulathromycin’ Text with EEA relevance
- 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 Text with EEA relevance
- Regulation (EC) No 470/2009 of the European Parliament and of the Council of 6 May 2009 laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No 726/2004 of the European Parliament and of the Council (Text with EEA relevance )
- 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 Text with EEA relevance
- Commission Regulation (EU) No 758/2010 of 24 August 2010 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 valnemulin Text with EEA relevance
- Commission Regulation (EU) No 914/2010 of 12 October 2010 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 Text with EEA relevance
- Council Directive 94/29/EC of 23 June 1994 amending the Annexes to Directives 86/362/EEC and 86/363/EEC on the fixing of maximum levels for pesticide residues in and on cereals and foodstuffs of animal origin respectively
- Commission Implementing Regulation (EU) 2019/238 of 8 February 2019 amending Regulation (EU) No 37/2010 to classify the substance ovotransferrin as regards its maximum residue limit (Text with EEA relevance.)
- 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 Text with EEA relevance
- Commission Implementing Regulation (EU) No 123/2012 of 13 February 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 monepantel Text with EEA relevance
- Commission Implementing Regulation (EU) 2015/149 of 30 January 2015 amending the Annex to Regulation (EU) No 37/2010 as regards the substance ‘methylprednisolone’ Text with EEA relevance
- Commission Implementing Regulation (EU) No 122/2012 of 13 February 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 methylprednisolone Text with EEA relevance
- 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 (Text with EEA relevance.)
- Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Union procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Text with EEA relevance)Text with EEA relevance
- 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 Text with EEA relevance
- Commission Implementing Regulation (EU) No 19/2014 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 chloroform Text with EEA relevance
- Commission Implementing Regulation (EU) 2016/305 of 3 March 2016 amending Regulation (EU) No 37/2010 as regards the substance ‘gentamicin’ (Text with EEA relevance)
- Commission Implementing Regulation (EU) No 85/2012 of 1 February 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 altrenogest Text with EEA relevance
- Commission Implementing Regulation (EU) No 86/2012 of 1 February 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 lasalocid Text with EEA relevance
- 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 (Text with EEA relevance. )
- European Parliament and Council Directive No 95/2/EC of 20 February 1995 on food additives other than colours and sweeteners
- 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 (Text with EEA relevance. )
- 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 Text with EEA relevance
