Veterinary drug consultations
Current Consultations
- Consultation: Categorization of antimicrobial drugs based on importance in human medicine [2025-06-18 - 2025-08-16]
- Consultation: Proposal to amend the list of maximum residue limits for veterinary drugs in foods - Proposed MRL 2025-1 [2025-02-05 - 2025-04-21]
- Consultation on the draft guidance for preparing veterinary abbreviated new drug submissions: Clinical and human safety requirements [2024-03-20 – 2024-05-19]
- Consultation on the draft guidance for preparing veterinary drug submissions: Quality requirements [2024-03-20 – 2024-05-19]
- Consultation: Proposal to amend the list of maximum residue limits for veterinary drugs in foods - Proposed MRL 2023-1 [2023-07-11]
- Consultation: Exceptions to the Prescription Drug List [2022-07-28]
- Consultation: Draft guidance on veterinary drug labelling [2022-03-07]
- Consultation to amend List A (List of certain antimicrobial active pharmaceutical ingredients) - Proposed List A 2022 [2022-03-07]
- Consultation: Veterinary drugs - Management of regulatory submissions: Updated guidance for industry [2021-05-14]
- Consultation on fee proposal for drugs and medical devices [2017-10-11]
- Consultation on VICH Guideline 58 [2018-08-10]
Past Consultations
- Share and view ideas: Proposal to Amend the List of Maximum Residue Limits for Veterinary Drugs in Foods - Proposed MRL 2018-1 [2018-03-08]
- Consultation on the Proposed Teat Antiseptic Product Monograph [2017-03-06]
- Consultation on VICH (International Cooperation on Harmonization of Technical Requirements for Registration of Veterinary Products) guideline 56: Studies to evaluate the Metabolism and Residue Kinetics of veterinary drugs in food-producing species: study design recommendations for residue studies in honey for establishing MRLs and withdrawal periods (step 4) [2017-02-15]
- Consultation on the Proposed Teat Antiseptic Product Monograph [2017-03-06]
- Consultation on VICH (International Cooperation on Harmonization of Technical Requirements for Registration of Veterinary Products) guideline 56: Studies to evaluate the Metabolism and Residue Kinetics of veterinary drugs in food-producing species: study design recommendations for residue studies in honey for establishing MRLs and withdrawal periods (step 4) [2017-02-15]
- Consultation on the Atypical Active Pharmaceutical Ingredients List [2016-12-02]
- Consultation on New Regulations for Antimicrobial Resistance Related to Veterinary Drugs [2016-07-14]
- Consultation - Revision to the Final Guidance Document on Classification of Veterinary Drugs and Livestock Feed [2015-11-27]
- Consultation on VICH guideline 52: Bioequivalence - Blood Level Bioequivalence Study (step 4) [2014-01-10]
- Consultation - Guidance Document on Classification of Veterinary Drugs and Animals Feeds [2013-02-06]
- Consultation on revised VICH guideline 23: Studies to Evaluate the Safety of Residues of Veterinary Drugs in Human Food: Genotoxicity testing (step 4) [2013-01-21]
- Consultation on the new Prescription Drug List [2012-12-24]
- Release of Quality Overall Summary - Chemical Entities (QOS-CE) for New Drug Submissions and Abbreviated New Drug Submissions and Certified Product Information Document - Chemical Entities (CPID-CE) [2012-11-01]
- Consultation on VICH guideline 51: statistical evaluation of stability data (step 4)