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Codex Committee on Residues of Veterinary Drugs in Foods (CCRVDF)

FAO/WHO ID No:CX-730
Reference:CX/RVDF
Terms of Reference:(a) to determine priorities for the consideration of residues of veterinary drugs in foods;
(b) to recommend maximum levels of such substances;
(c) to develop codes of practice as may be required; and,
(d) to consider methods of sampling and analysis for the determination of veterinary drug residues in foods.
Status:Active
Host:United States of America

Related Circular Letters

Code Issued Title Deadline EN FR ES AR ZH RU
CL 2010/47-RVDF08/10Distribution of the Report of the Nineteenth Session of the Codex Committee on: PART C . REQUEST FOR COMMENTS29/11/2011
CL 2010/50-RVDF08/10Request for comments/information on Priority List of Veterinary Drugs Requiring Evaluation or Reevaluation14/12/2011
CL 2012/11-RVDF04/12Distribution of the Report of the Twentieth Session of the Codex Committee on Residues of Veterinary Drugs in Foods (REP12/RVDF)14/06/2012
CL 2012/23-RVDF07/12Request for comments on:Part A: Comments at Step 6 on the draft Maximum Residue Levels (MRLs) for Monepantel (sheep tissues)Part B: Comments at Step 3 on the proposed draft Risk Management Recommendations for Chloramphenicol and Malachite green (N10-2012)29/05/2013
CL 2012/30-RVDF09/12Request for comments/information on priority list of veterinary drugs for evaluation or reevaluation by JECFA29/05/2013
CL 2013/26-RVDF08/13Distribution of the Report of the Twenty-First Session of the Codex Committee on Residues of Veterinary Drugs in Foods (REP14/RVDF)29/03/2014
CL 2014/03-RVDF12/13Request for Comments/Information on Priority List of Veterinary Drugs for Evaluation or Reevaluation by JECFA14/12/2014
CL 2014/09-RVDF02/14Request for Revision/Information to the Database on Countries' Needs for MRLs29/06/2014
CL 2015/18-RVDF06/15Request for comments / information on priority list of veterinary drugs for evaluation or reevaluation by JECFA 15/08/2016
CL 2015/14-RVDF05/15PART B – Request for Comments at step 3: Proposed Draft Risk Management Recommendation for Gentian Violet31/07/2016
CL 2016/38/OCS-RVDF10/16Request for comments at Step 5/8 on the proposed draft MRLs for lasalocid sodium, ivermectin and teflubenzuron15/06/2017
CL 2016/39/OCS-RVDF10/16Request for comments at Step 5 on the proposed draft RMR for gentian violet 15/06/2017
CL 2016/42-RVDF12/16Request for Revision/Information to the Database on Countries’ Needs for MRLs15/12/2017
CL 2016/41-RVDF12/16Request for Comments/Information on Priority List of Veterinary Drugs for Evaluation or Reevaluation by JECFA15/02/2018
CL 2017/72/OCS-RVDF08/17Request for comments at Step 6 on the draft RMR for gentian violet30/01/2018
CL 2017/85/OCS-RVDF12/17Request for comments at Step 3 on the proposed draft MRLs for amoxicillin (finfish fillet, muscle); ampicillin (finfish fillet, muscle); flumethrin (honey), lufenuron (salmon and trout fillet), monepantel (cattle fat, kidney, liver, muscle)15/03/2018
CL 2018/36/OCS-RVDF05/18Request for comments at Step 8 on the draft Risk Management Recommendation for Gentian Violet 10/06/2018
CL 2018/37/OCS-RVDF05/18Request for comments at Step 5/8 on the proposed draft maximum residue limits for veterinary drugs: Amoxicillin (finfish fillet, muscle); Ampicillin (finfish fillet, muscle); Alufenuron (salmon and trout fillet) and Monepantel (cattle fat, kidney, liver, muscle) 10/06/2018
CL 2018/38/OCS-RVDF05/18Request for comments at Step 5 on the proposed draft maximum residue limit for flumethrin (honey)10/06/2018
CL 2020/17(REV1)-RVDF02/20Request for comments on MRLs for veterinary drugs tissues28/02/2021
CL 2020/18(REV1)-RVDF02/20Request for comments on the priority list of veterinary drugs for evaluation by JECFA28/02/2021
CL 2020/42(REV1)-RVDF07/20Request for comments / information on the: (i) approach for the extrapolation of MRLs for veterinary drugs to one or more species and (ii) proposals for MRLs based on the approach proposed for extrapolation of MRLs to one or more species28/02/2021
CL 2021/02/OCS-RVDF0/Request for comments on the recommendations for the further steps on the use and maintenance of the database on countries’ needs for maximum residue limits for veterinary drugs in foods30/04/2021
CL 2021/05/OCS-RVDF01/21Request for comments on the principles and procedure for the parallel review of a new veterinary drug by JECFA and national regulatory agencies 30/04/2021
CL 2021/06/OCS-RVDF04/21Request for comments on the recommendations for edible offal and other animal tissues of relevance for the purpose of harmonization and elaboration of maximum residue limits for compounds with dual uses05/06/2021
CL 2021/75-RVDF10/21Request for comments on texts going for adoption by CAC (Steps 5, 5/8 and 8) – CCRVDF05/11/2021
CL 2021/98-RVDF12/21Request for comments on proposed MRLs for veterinary drugs extrapolated to one or more species25/03/2022
CL 2022/71-RVDF0/Request for comments at Steps 3 and 6 on MRLs for veterinary drugs05/01/2023
CL 2022/72-RVDF0/Request for comments/information on the priority list of veterinary drugs for evaluation or re-evaluation by JECFA10/01/2023
CL 2022/76-RVDF0/Request for comments on the extrapolation of MRLs for veterinary drugs to one or more species30/01/2023
CL 2022/77-RVDF12/22Request for comments on criteria and procedures for the establishment of action levels for unintended and unavoidable carryover of veterinary drugs from feed to food of animal origin30/01/2023
CL 2022/78-RVDF12/22Request for comments on the recommendations arising from the Joint CCPR/CCRVDF EWG 30/01/2023
CL 2022/79-RVDF0/Request for comments on conclusions/recommendations concerning issues pertaining to harmonization of edible offal0/0/
CL 2024/65-RVDF07/24Request for comments on MRLs for veterinary drugs in foods30/09/2024
CL 2024/66-RVDF07/24Request for comments/information on the priority list of veterinary drugs for evaluation or re-evaluation by JECFA30/09/2024
CL 2024/67-RVDF07/24Request for comments on extrapolation of MRLs for veterinary drugs to one or more species30/09/2024
CL 2024/68-RVDF08/24Request for comments on criteria and procedures for the establishment of action levels for veterinary drugs in food of animal origin resulting from unavoidable and unintentional veterinary drug carry-over in non-target animal feed05/10/2024