Guidelines and Forms
Group 1, Group 2, Group 3, Group 4
Group 1 - Legislation pertaining to Veterinary Biologics
1.3
Canadian Food Inspection Agency Fees Notice - Part 11, Health of Animals Fees
1.4
Veterinary Biologics Program Service Standards (Response Times)
Group 2 - Veterinary Biologics Forms
2.1
CFIA/ACIA 4720 - Application for Services - PDF (311 kb)
2.2
2.3
2.4
2.5
2.6
CFIA/ACIA 5212 - Revisions to Outlines of Production and Special Outlines for Veterinary Biologics - PDF (165 kb) (Licensed in the United States)
2.7
2.8
2.9
Veterinary Biologics Templates
New Product Submission Checklist
Group 3 - Guidelines and Information on Veterinary Biologics
3.1
3.2
Guideline for Regulation of Biotechnology-Derived Veterinary Biologics
3.3
Guideline for Labelling of Veterinary Biologics
3.4
3.5
Guideline for Advertising of Veterinary Biologics
3.6
3.7
3.11
3.13
Guideline for Autogenous Veterinary Biologics
3.15
3.16
Guideline for Registration of Immunoglobulin Supplements
3.17
Guideline for Reporting Laboratory and Field Efficacy Trials
3.19
Guideline for Licensing Veterinary Diagnostic Test Kits in Canada
3.21
3.22
3.23
Guideline for Licensing Veterinary Nucleic Acid Vaccines
3.24
Guideline for Inspection of Veterinary Biologics Importers
3.26
Guideline for Issuance of Veterinary Biologics Export Certificates
3.28
Guideline for Personnel Requirements
3.29
Guideline for Safety Requirements for Veterinary Biologics
3.31
3.32
3.33
Guideline for Commercial Importers of Veterinary Biologics in Canada
Group 4 - References
Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH)
Although the CCVB intends to adopt VICH guidelines as primary guidance documents, they are to be viewed as administrative instruments and not specified requirements of the Health of Animals Act and Regulations and therefore allow for flexibility of approach.
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