Codex Committee on residues of veterinary drugs
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:

• Item 2: Matters Referred by the Codex Alimentarius Commission and Other Codex Committees and Task Forces
• Item 3: Matters arising from FAO/WHO and from the 75th Meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA )
• Item 6: Draft Maximum Residue Limits (MRLs) for Veterinary Drugs
• Item 7 b) : 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
• Item 8 a): Proposed draft Sampling Plans for Residue Control for Aquatic Animal Products and Derived Edible Products of Aquatic Origin
• Item 8 b): Proposed draft Guidelines on performance characteristics for multi-residues methods
• 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
• Item 11: Discussion paper on the policy for the establishment of MRLs or other limits in honey
• Item 12: Discussion paper on extrapolation of MRLs to additional species and tissues

European Union comments on:

• 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
  

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