Compare
Compare archived captures
This view highlights text differences between two archived captures. It does not interpret meaning or provide guidance.
Descriptive changes only
This comparison highlights text changes between archived captures. It does not interpret the change or provide medical advice. For up-to-date recommendations, always consult the official source website.
Need to cite this comparison? See /cite.
Earlier capture
Veterinary drug consultations - Canada.ca
Apr 18, 2025
legacy-hc-2025-04-21
ID 202222
Later capture
Veterinary drug consultations - Canada.ca
Jan 2, 2026
hc-20260101
ID 429079
updated3 sections changed
3 sections changed0 added0 removed+3 / -12 linesChange ratio: 15%
--- +++ @@ -1,5 +1,7 @@ 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residue limits for veterinary drugs in foods - Proposed MRL 2025-1 [2025-02-05 - 2025-04-21] Consultation on the draft guidance for preparing veterinary abbreviated new drug submissions: Clinical and human safety requirements@@ -25,29 +27,18 @@ [2018-03-08] Consultation on the Proposed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) Page details-Date modified:-2025-02-05+2025-06-18