► Regulation (EU) 2024/2052 : of 30 July 2024 amending Implementing Regulation (EU) 2021/808 as regards its scope and certain performance criteria of analytical methods for residues of pharmacologically active substances used in food-producing animals;  

► Regulation (EU) 2024/1229 : of 20 February 2024 supplementing Regulation (EU) 2019/4 of the European Parliament and of the Council by establishing specific maximum levels of cross-contamination of antimicrobial active substances in non-target feed and methods of analysis for these substances in feed;  

► Regulation (EU) 2022/1646 : of 23 Septembre 2022 on uniform practical arrangements for the performance of official controls as regards the use of pharmacologically active substances authorised as veterinary medicinal products or as feed additives and of prohibited or unauthorised pharmacologically active substances and residues thereof, on specific content of multi-annual national control plans and specific arrangements for their preparation;    

► Regulation (EU) 2022/1644 : of 7 July 2022 supplementing Regulation (EU) 2017/625 of the European Parliament and of the Council with specific requirements for the performance of official controls on the use of pharmacologically active substances authorised as veterinary medicinal products or as feed additives and of prohibited or unauthorised pharmacologically active substances and residues thereof;   

► EURL GUIDANCE : EURL Guidance Document on standard addition in the field of the analysis of residues of pharmacologically active substances  Version 1.1 of  29 November 2022  

► EURL GUIDANCE : EURL “MMPR” GUIDANCE FOR SPECIFIC PHARMACOLOGICALLY ACTIVE SUBSTANCES IN SPECIFIC ANIMAL MATRICES Version 2.0 of June 2022 repealing Version 1 of September 2020 (Guidance updated in 2025)

► EURL GUIDANCE : EURL Guidance Document on the Quality Control during routine analysis (ongoing performance verification) Version 1.1 of 8 October 2020

► MMPR – EURL GUIDANCE : EURL guidance on minimum method performance requirements (MMPRs) for specific pharmacologically active substances in specific animal matrices version 1 of September 2020 repealing the “CRL Guidance Paper” of 7 December 2007  (Guidance updated in 2022)

► RPA – EFSA Scientific opinion update : methodological principles and scientific methods to be taken into account when establishing RPAs for non-allowed pharmacologically active substances present in food of animal origin

► Regulation (EU) 2018/470 : on detailed rules on the MRL to be considered for contol purposes for foodstuffs dervied from animals which have been treated in the EU under Article 11 of Directive 2001/82/EC - The Cascade Use

► RPA - Scientific Opinion of EFSA-CONTAM on Malachite Green

► RPA - Scientific Opinion of EFSA-CONTAM on Chloramphenicol

► Document SANCO/2014/10047 (update 2014) : amending Decision 98/536/EC establishing the list of national reference laboratories for the detection of residues

► Regulation (EU) 208/2011 (update 2011) : amending Annex VII to Regulation (EC) No 882/2004 of the European Parliament and of the Council and Commission Regulations (EC) No 180/2008 and (EC) No 737/2008 as regards lists and names of EU reference laboratories

► Regulation (EC) 470/2009 : 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

► CRL Guidance Paper of 7 dec 2007 : CRLs VIEW ON STATE OF THE ART ANALYTICAL METHODS FOR NATIONAL RESIDUE CONTROL PLANS

► Decision (EC) 181/2003 : the setting of minimum required performance limits(MRPLs) for certain residues in food of animal origin - case of chloramphenicol, nitrofurans and medroxyprogesterone

► Directive (EC) 2001/82 :  on the Community code relating to veterinary medicinal products