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Animals > Veterinary Biologics > Guidelines / Forms 

Guidelines / Forms

Group 1 - Legislation pertaining to Veterinary Biologics
1.1 Health of Animals Act
1.2 Health of Animals Regulations
1.3 Financial Administration Act
1.4 Canadian Food Inspection Agency Fees Notice - Part 11, Health of Animals Fees
1.5 Veterinary Biologics Program Service Standards (Response Times)
Veterinary Biologics Check-Lists
New product submission check-list
New product submission check-list for diagnostic kits
Veterinary Biologics Templates
Manufacturer's Serial Release Test Report to VBS

Group 2 - Veterinary Biologics Forms
2.1 Application for Services (CFIA/ACIA 4720) - PDF
2.2 Application for Permit to Import Veterinary Biologics into Canada (CFIA/ACIA 1493) - PDF
2.3 Veterinary Biologics Information Form (CFIA/ACIA 1503) - PDF
2.4 Permit to Import Veterinary Biologics (CFIA/ACIA 5067)
2.5 Veterinary Biologics Establishment Licence (CFIA/ACIA 1589)
2.6 Veterinary Biologics Product Licence (CFIA/ACIA 4602)
2.7 Notification of Suspected Adverse Events to Veterinary Biologics (CFIA/ACIA 2205) - PDF
2.8 Summary of Fees and Services Related to Veterinary Biologics (CFIA/ACIA 5189) - PDF
2.9 Revisions to Outlines of Production and Special Outlines for Veterinary Biologics (Licensed in the United States) (CFIA/ACIA 5212) - PDF
2.10 Application for Renewal of Veterinary Biologics Product Registration and Import Permit (CFIA/ACIA 5213) - PDF
2.11 Application for Renewal of Veterinary Biologics Establishment Licence and Product Licence (CFIA/ACIA -5214) - PDF

Group 3 - Guidelines and Information on Veterinary Biologics
3.1 Summary of Requirements and Guidelines for Veterinary Biologics in Canada
3.2 Guidelines for the Regulation of Veterinary Biologics Produced by Biotechnology
3.3 Guidelines for Labelling of Veterinary Biologics
3.5 Guidelines for Advertising of Veterinary Biologics
3.6 Guidelines for Bluetongue Virus Exclusion Test for Veterinary Biologics
3.7 Guidelines for Preparation of Production Outlines, Special Outlines, and Summary of Changes for Veterinary Biologics
3.8 Guidelines for Autogenous Veterinary Biologics for Use in Fish
3.10 Guidelines for the Manufacture of Veterinary Biological Products, Including Those for Export
3.11 Guidelines for Inspection of Veterinary Biologics Manufacturers and Importers
3.12 Veterinary Biologics Product Review Guidelines
3.13 Guidelines for Autogenous Veterinary Biologics
3.15 Guidelines for Reporting Suspected Adverse Events to Veterinary Biologics
3.16 Guidelines for Registration of Immunoglobulin Supplements
3.17 Guide for Reporting Laboratory and Field Efficacy Trials
3.18 Cost Recovery Fees for Veterinary Biologics - Questions & Answers
3.19 Guidelines for Licensing Veterinary Diagnostic Test Kits in Canada
3.21 Guidelines for the Importation of Veterinary Biologics for Research or Emergency Use
3.22 Guidelines for the Submission, Testing and Reporting of Biological Samples
3.23 Guidelines for Licensing Veterinary Nucleic Acid Vaccines
3.24 Guidelines for Inspection of Veterinary Biologics Importers
3.25 Guidelines for Importation of Veterinary Biologics

Group 4 - References
4.1 Public Health Agency of Canada Laboratory Biosafety Guidelines
4.3 Canadian Council on Animal Care (CCAC) Guidelines
4.4 Codes of Practice for Care of Farm Animals
4.5 Licensing Requirements for Veterinary Biologics in Canada
4.6 Risk Analysis for Veterinary Biologicals Released into the Environment
4.7 Containment Standards for Veterinary Facilities (1921/E)
4.8 Safety Requirements for Veterinary Biological Products in Canada
4.9 Veterinary Biologics Licensing Information - Canada (contacts)
4.10 The Regulation of Veterinary Biologics in Canada


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