21st Session
Minneapolis, Minnesota, United States of America, 26–30 August 2013
European Union comments on:
- Agenda item 6: Risk Management Recommendations for Residues of Veterinary Drugs for which no ADI and/or MRL has been recommended by JECFA due to Specific Human Health Concerns
- Agenda item 7: Proposed draft Guidelines on performance characteristics for multi-residues methods
- Agenda item 8b: Proposed "concern form" for the CCRVDF (Format and policy procedure for its use)
20th Session
San Juan, Puerto Rico, 7-11 May 2012
- Annotated Agenda indicating the division of Competence between the European Union and its Member States according to Rule of Procedure II Paragraph 5 of the Codex Alimentarius Commission.
European Union comments on:
- Agenda item 2: Matters Referred by the Codex Alimentarius Commission and Other Codex Committees and Task Forces
- Agenda item 3: Matters arising from FAO/WHO and from the 75th Meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA)
- Agenda item 6: Draft Maximum Residue Limits (MRLs) for Veterinary Drugs
- Agenda item 7b: Proposed revision of Risk Analysis Principles applied by the CCRVDF and the Risk Assessment Policy for the setting of maximum limits for residues of veterinary drugs in foods
- Agenda item 8a: Proposed draft Sampling Plans for Residue Control for Aquatic Animal Products and Derived Edible Products of Aquatic Origin
- Agenda item 8b: Proposed draft Guidelines on performance characteristics for multi-residues methods
- Agenda item 10 :Risk management recommendations for the veterinary drugs for which no ADI and/or MRL has been recommended by JECFA due to specific human health concerns
- Agenda item 11: Discussion paper on the policy for the establishment of MRLs or other limits in honey
- Agenda item 12: Discussion paper on extrapolation of MRLs to additional species and tissues
- CL 2010/47-RVDF - Part C: Request for Comments on the Proposed amendments to the Risk Analysis Principles applied by Codex Committee on Residues of Veterinary Drugs in Foods and the Proposed Amendments to the Terms of Reference of the Codex Committee on Residues of Veterinary Drugs in Foods
19th Session
Burlington, Vermont, United States of America, 30 August – 3 September 2010
- Annotated Agenda indicating the division of Competence between the European Union and its Member States according to Rule of Procedure II Paragraph 5 of the Codex Alimentarius Commission.
European Union comments/data on:
- Agenda item 2: Matters Referred by the Codex Alimentarius Commission and Other Codex Committees and Task Forces
- Agenda item 8: Factors taken into account in connection with establishing the ADI and the current process of recommending MRLs
- Agenda item 10: Discussion Paper on Veterinary Drugs in Honey Production
- CL 2009/22-RVDF: Draft Codex MRLs for narasin in cattle and pig tissues and for tilmicosin in chicken and turkey tissues.
- CL 2009/21-RVDF "Requests for information and comments on veterinary drugs registered for honey production and bee health, honey consumption and good veterinary practices in honey production" - Codex document - "Bee products: situation in Europa " - "Gross human apparent consumption of main food items "
18th Session
Natal, Brazil, 11-15 May 2009
- Annotated Agenda for the Codex Committee on Residues of Veterinary Drugs.
European Union comments on:
- Agenda Item 2: "Matters Referred by the Codex Alimentarius Commission and Other Codex Committees and Task Forces - Draft Codex MRLs for Ractopamine"
"EFSA Scientific Opinion and Safety Evaluation of Ractopamine " , published by the Panel on Additives and Products or Substances used in Animal Feed , adopted on 2 April 2009. - Agenda item 3: Matters of Interest arising from FAO/WHO and from the 70th Meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA)
- Agenda item 5a: MRLs for melengestrol acetate
- Agenda item 5b: Proposed draft MRLs for Veterinary Drugs (at step 3)
- Agenda item 6: Draft Guidelines for the Design and Implementation of National Regulatory Food Safety Assurance Programmes Associated with the Use of Veterinary Drugs in Food Producing Animals
- Agenda item 7: Discussion Paper on consideration of methods of analysis and sampling in CCRVDF
- Agenda item 8: Draft Priority list of veterinary drugs requiring evaluation of re-evaluation by JECFA
17th Session
Breckenridge, Colorado, United States 3-7 September 2007
- Annotated Agenda indicating the division of competence and right to vote between the European Community and its Member States in respect of each particular agenda item.
European Community comments on:
- Agenda Items 2, 3 a) and 5 (CRD 14):
- Agenda Item 10: "Risk Management Topics and Options for the CCRVDF"
- CL 2007/4-RVDF: "Proposed draft methods of analysis for veterinary drug residues" Codex Document
- CL 2006/35-RVDF: "i) Draft Maximum Residue Limits for Veterinary Drugs (colistin and ractopamine)" - Codex Document
- CL 2006/35-RVDF: "Request for Comments at Steps 6 of the Procedure on: ii) Draft Guidelines for the Design and Implementation of National Regulatory Food Safety Assurance Programmes Associated with the Use of Veterinary Drugs in Food Producing Animals." - Codex Document
16th Session
Cancun, Quintana Roo, Mexico, 8 -12 May 2006
- Annotated agenda indicating the division of competence and right to vote between the European Community and its Member States in respect of each particular agenda item.
European Union comments on:
- Cx/Rvdf 06/16/8: Proposed Draft Revised Guidelines for the Establishment of a Regulatory Program for the Control of Veterinary Drug Residues in Foods -Codex Document
- Cx/Rvdf 06/16/9: Proposed Draft Revised Part I, Ii, Iii of the Codex Guidelines for the Establishment of a Regulatory Program for the Control of Veterinary Drug Residues in Foods -Codex Document
- Agenda Item 6d: Draft and proposed MRLs for Veterinary Drugs (at Step6 and Step 3 of the Procedure).
- CL 2005/35-RVDF: "Draft Maximum Residue Limits for Veterinary Drugs" (flumequine, pirlimycin, cypermethrin and alpha-cypermethrin and doramectin) (Appendices V of ALINORM 05/28/31).
Codex Document - CL 2005/10-RVDF - Methods of analysis for veterinary drug
- CL 2004/50-RVDF - Part C: Veterinary Drugs without ADI/MRL. ( annex 1 ) (annexe 2 )
15th Session
Washington DC, United States of America, 26-29 October 2004
- Annotated Agenda for the 15th session of the Codex Committee on Residues of Veterinary Drugs in Foods
European Union comments on:
- Agenda Item 3: CX/RVDF 04/15/2 - Chapter 6.
- Agenda Item 7: "Proposed Draft Code of Practice to Minimise and Contain Antimicrobial Resistance" - CL 2003/40 RVDF
- Agenda Item 8: Codex Guidelines for the Establishment of a Regulatory Programme for Control of Veterinary Drug Residues in Foods (CX/RVDF 04/15/6)
- Agenda Item 9: Part II "General Considerations on Analytical Methods for Residues Control" of the Guidelines for the Establishment of a Regulatory Programme for Control of Veterinary Drugs Residues in Foods (CAC/GL 16-1993) (CX/RVDF 04/15/7)
- REVISED comments on CL 2003/24 - RVDF: "Report of the 14th session of the Codex Committee on Residues of Veterinary Drugs in Foods" (ALINORM 03/41)
- CL 2004/17 - RVDF:
(a) Recommendations on maximum residue limits from the 60th and 62nd meetings of JECFA
(b) Priority list of veterinary drugs for evaluation or re-evaluation - CL 2003/24 - RVDF: "Report of the 14th session of the Codex Committee on Residues of Veterinary Drugs in Foods" (Alinorm 03/41) - Request for comments
- Agenda Item 13a: "Discussion Paper on Rounding of ADIs for Veterinary Drugs prior to the Setting of MRLs."
14th Session
Washington - 4-7 March 2003
European Union comments on:
- Document CX/RVDF 03/5: Agenda Item 6: Proposed Draft Appendix on the Prevention and Control of Veterinary Drug Residues in Milk and Milk Products
- Document CX/RVDF 03/6: Agenda Item 7: Draft Code of Practice to Minimize and Contain Antimicrobial Resistance
- Document CX/RVDF 03/8: Discussion Paper on Risk Management Methodologies, including risk assessment policies in the Codex Committee on Residues of Veterinary Drugs in Food
- CX/RVDF 03/9: Agenda Item 10: Discussion Paper on Residue Issues for the Codex Committee on Residues of Veterinary Drugs in Foods
- Document CX/RVDF 03/10: Agenda Item 11 a: Review of Performance-Based Criteria for Methods of Analysis for Veterinary Drug Residues in Foods
- CL 2001/49 - RVDF
Report of the 13th session of the Codex Committee on Residues of Veterinary Drugs in Foods (Alinorm 03/31) - CL 2001/49 - RVDF Part A: "Matters for Adoption by the 25th Session of the Codex Alimentarius Commission at Step 8, Step 5/8 or Step 5 under the accelerated Procedure"
- CL 2002/32 - RVDF
Request for Comments at Step 6 on Draft Standard and Related Texts of the Codex Committee on Residues of Veterinary Drugs in Foods - CL 2002/34 - RVDF
Request for Comments
a) Recommendations on maximum residue limits from the 58th meeting of JECF;
b) Priority list of veterinary drugs for evaluation or re-evaluation - CL 2003/11 - RVDF: Parts A and B
13th Session
Charleston, South Carolina, USA, 4-7 December 2001
European Union comments on:
- CX/RVDF 01/08 - Agenda Item 08: Control of Veterinary Drug Residues in Milk and Milk Products
- CX/RVDF 01/09 - Agenda Item 09: Discussion Paper on Risk Analysis Principles and Methodologies in the CCRVDF
- CX/RVDF 01/11 - Agenda Item 11: Discussion Paper on Residue Issues for the Codex Committee on Residues of Veterinary Drugs in Foods
- CX/RVDF 01/12 - Agenda Item 12: Review of performance based criteria for methods of analysis for veterinary drug residues in foods
- CL 2000/28-RVDF: Request for comments at steps 6 and 3 on draft and proposed draft MRLs for veterinary drugs - Annex
- CL 2000/23-RVDF: Request for comments on the priority list of veterinary drugs requiring evaluation or re-evaluation
- CL 2000/28-RVDF: Request for comments at steps 6 and 3 on draft and proposed draft MRLs for veterinary drugs
- European Community Position - Follow-up of 12th CCRVDF meeting: Scientific justifications for certain positions of the European Community - Annex
12th Session
Washington, D.C., 28-31 March 2000
European Union comments on:
- Agenda item 3: Matters Referred from the Codex Alimentarius Commission and Other Codex Committees - Draft maximum limits for bovine somatotropin (BST) - CX/RVDF 00/2, CX/RVDF 00/6 and ALINORM 99/31 paragraphs 65-70
- Agenda item 3: Matters Referred from the Codex Alimentarius Commission and Other Codex Committees - Other legitimate factors - CX/RVDF 00/2
- Agenda item 4: Risk Analysis Principles and Methodologies of the Codex Committee on Residues of Veterinary Drugs in Foods - CX/RVDF 00/3 and Appendix IX of ALINORM 99/31)
- Agenda item 5: Antimicrobial resistance and the use of antibiotics in animal production - CX/RVDF 00/4
- Agenda item 8.2: Harmonization of MRL setting for compounds used both as pesticides and as veterinary drugs - CX/RVDF 00/7
- Agenda item 9a: Methods of Analysis for Veterinary Drugs - Review of Performance-based Criteria for Methods of Analysis and Sampling for Veterinary Drug Residues in Foods - CX/RVDF 00/9 and CX/RVDF 00/10
- Agenda item 9b: Identification of Routine Methods of Analysis and Sampling for Veterinary Drug Residues in Foods
- Agenda item 11: Control of Veterinary Drugs in Milk and Milk products
- Agenda item 9b - Annex: Methods of Analysis for Veterinary Drugs
- CL 1999/13 GEN: Consideration of maximum residue limits at steps 6 (7)
- CL/1999 14-RDVF: Nomination of Priority Substances for Future Evaluation by JECFA
- CL/1999 14-RDVF: Nomination of Priority Substances for Future Evaluation by JECFA: Summary of Residue assessments in the EC
- CX/RVDF 00/06: Consideration of maximum residue limits at steps 7 and 4
- CX/RVDF 00/14: Discussion Paper on Data Requirements for the Establishment of Maximum Residue Limits for Veterinary Drugs for Minor Species