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Veterinary Biologics
Main Page - Animal Products
Main Page - Veterinary Biologics
Acts
&
Regulations
Reference Material
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Veterinary Biological Products licensed in Canada
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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)
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PDF
2.2
Application for Permit to Import Veterinary Biologics into Canada (CFIA/ACIA 1493)
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PDF
2.3
Veterinary Biologics Information Form (CFIA/ACIA 1503)
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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)
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PDF
2.8
Summary of Fees and Services Related to Veterinary Biologics (CFIA/ACIA 5189)
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PDF
2.9
Revisions to Outlines of Production and Special Outlines for Veterinary Biologics (Licensed in the United States) (CFIA/ACIA 5212)
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PDF
2.10
Application for Renewal of Veterinary Biologics Product Registration and Import Permit (CFIA/ACIA 5213)
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PDF
2.11
Application for Renewal of Veterinary Biologics Establishment Licence and Product Licence (CFIA/ACIA -5214)
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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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