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Drugs and Health Products
What's New
- Consultation on VICH guideline 46: Studies to evaluate the Metabolism and Residue Kinetics of Veterinary Drugs in Food-producing Animals: Metabolism Study to determine the Quantity and Identify the Nature of Residues (step 4). [2010-03-17]
- Consultation on VICH guideline 47: Studies to evaluate the metabolism and residue kinetics of veterinary drugs in food-producing animals: Comparative metabolism studies in laboratory animals (step 4) [2010-03-17]
- Consultation on VICH guideline 48: Studies to evaluate the Metabolism and Residue Kinetics of Veterinary Drugs in Food-producing Animals: Marker Residue Depletion Studies to establish Product Withdrawal Periods (step 4) [2010-03-17]
- Consultation on VICH guideline 49: Guidelines for the Validation of Analytical Methods used in Residue Depletion Studies (step 4) [2010-03-17]
- Consultation - Maximum residue limit (MRL) proposal for Amoxicillin, Neomycin, Ormetoprim, Tetracycline, Chlortetracycline, Oxytetracycline, Tilmicosin, Tricaine Methanesulfonate, Tulathromycin and Zoalene [2010-03-12]
- Guidance for Industry - Preparation of Veterinary Abbreviated New Drug Submissions - Generic Drugs [2010-03-01]
- Food and Drug Regulations - Project Number 1621 - Schedule F Amendment [2010-02-01]
- Health Canada Advises Canadians About Problems with Insulin Product for Dogs and Cats [2009-11-19]
- Notice - Post-Notice of Compliance (NOC) Changes Guidance Documents [2009-09-30]
- Guidance Document on Post-Drug Identification Number (DIN) Changes [2009-09-29]
- Antimicrobial Categorization document - Results of consultation [2009-09-23]
- Questions and Answers on Health Canada's Policy on Extra-Label Drug Use (ELDU) in food-producing animals [2009-09-23]
- French-English Lexicon for Standard Labelling Statements [2009-08-04]
- Notice to Stakeholders: Guidance Document - Reconsideration of Decisions Issued for Veterinary Drug Submissions [2009-07-22]
- Submissions Containing Clinical Data from Studies Conducted outside of Canada [2009-06-16]
- Consultation on the Release of a draft revised Health Canada 3011: Drug Submission Application Form for Human, Veterinary, Disinfectant Drugs and Clinical Trial Application/Attestation [2009-05-01]
- Guidance Document: Data Protection under C.08.004.1 of the Food and Drug Regulations [2009-03-24]
Prudent Use of Veterinary Drugs in Livestock Feeds - Fact Sheet [2009-02-09]- Final Report of the Task Force on Own-Use Importation of Veterinary Drugs [2008-12-30]
- Draft Guidance Document - Drug Master Files (DMFs) [2008-09-05]
- Policy on Extra-Label Drug Use (ELDU) in food producing animals [2008-04-10]
- Fentanyl Transdermal Pain Patches recalled due to health risk [2008-03-17]
- Consultation Summary Report on the Draft Definition of a Veterinary Natural Health Product [2008-02-19]
- Call Out for the Establishment of an Expert Advisory Committee for Veterinary Natural Health Products [2008-02-19]
- Guidelines for Submitting a Nominee for the Expert Advisory Committee on Veterinary Natural Health Products (EAC-vNHP) [2008-02-19]
- Terms of Reference [2008-02-19]
- Closer ties on medicines safety between European and Canadian regulatory authorities [2008-01-11]
- Regulations Amending Certain Regulations Made under the Food and Drugs Act - Project 1539 (SOR/2007-288) [2007-12-27]
- Regulations Amending Schedule A to the Food and Drugs Act and the Medical Devices Regulations - Project 1539 (SOR/2007-289) [2007-12-27]
- Information to Veterinarians and horse owners on the discontinuation of the sale of Permax (pergolide mesylate) [2007-09-11]
- Document for Consultation Definition of a Veterinary Natural Health Product [2007-08-03]
- Draft Guidance Document: Data Protection under C.08.004.1 of the Food and Drug Regulations [2007-06-25]
- Drug Submission Tracking System - Industry Access (DSTS-IA) [2007-04-30]
- New Drug Submission Screening Form [2007-03-23]
- Proposal for Amoxicillin [2007-03-05]
- Proposal for Tulathromycin [2007-03-05]
- Guidance for Industry Preparation of Veterinary New Drug Submissions [2007-03-23]
- Consultation on Health Canada's Proposed Aquaculture Policy - Ensuring that Safe and Effective Veterinary Drugs are Available for Use in Aquatic Animal Species: A Policy Discussion Document [2007-03-23]
- Charting A Course: Refining Canada's Approach to Regulating Natural Health Products [2007-03-19]
- Notice - Post-Notice of Compliance (NOC) Changes [2007-03-16]
- Draft Guidance Document - Post-Notice of Compliance (NOC) Changes: Framework Document [2007-03-16]
- Draft Guidance Document - Post-Notice of Compliance (NOC) Changes: Safety & Efficacy Document [2007-03-16]
- Draft Guidance Document - Post-Notice of Compliance Changes: Quality Document [2007-03-16]
- Subject: Consultation on draft guidance for industry: Reconsideration of decisions issued for Veterinary Drug Submissions [2007-02-22]
- AMR Bulletin - Winter 2007 [2007-02-21]
