Canadian Food Inspection Agency
www.inspection.gc.ca
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About the CFIA
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Subjects
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Proactive Disclosure
Send this page by
emailGuidelines 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
Application for Services - CFIA/ACIA
4720
2.2
Application for Permit to Import
Veterinary Biologics into Canada - CFIA/ACIA 1493
2.3
Veterinary Biologics Information Form
- CFIA/ACIA 1503
2.4
Notification of Suspected Adverse Events
to Veterinary Biologics - CFIA/ACIA 2205
2.5
Summary of Fees and Services Related to
Veterinary Biologics - CFIA/ACIA 5189
2.6
Revisions to Outlines of Production and
Special Outlines for Veterinary Biologics (Licensed in the United States) - CFIA/ACIA 5212
2.7
Veterinary Biologics Templates
New Product Submission Checklist
Manufacturer's Serial Release Test Report
Group 3 - Guidelines and Information on Veterinary Biologics
3.1
Summary of Requirements and a Guideline for New Product Submissions for
Veterinary Biologics in Canada
3.2
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
3.18
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
3.25
Guideline for Importation of Veterinary Biologics
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
