Guidance Document Repository

The CFIA is responsible for regulating the safety and quality of food, animal and plant health in Canada. CFIA's official Guidance Documents provide the Agency's functional direction to its front line staff regarding their compliance verification activities. They also provide guidance to regulated parties regarding program requirements.

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Guidance Repository Search Results

Document Name Activities Date modified Type
VICH - The International Cooperation on Harmonization of Technical Requirements for the Registration of Veterinary Medicinal Products Additional Information 2014-06-02 HTML
Veterinary Biologics - Questions and Answers Additional Information 2017-08-25 HTML
Veterinary Biologics Guideline 4.5E
Licensing Requirements for Veterinary Biologics in Canada
Additional Information 2015-04-13 HTML
Veterinary Biologics Guideline 4.10E
The Regulation of Veterinary Biologics in Canada
Additional Information 2012-02-02 HTML
Manufacturer's Serial Release Test Report Additional Information 2012-02-02 HTML
New Product Submission Checklist - Vaccines Additional Information 2013-11-18 HTML
New Product Submission Checklist - Autogenous Vaccines Additional Information 2013-11-18 HTML
New Product Submission Checklist - Antibody Products Additional Information 2013-11-18 HTML
New Product Submission Checklist - Diagnostic Kits Additional Information 2013-11-18 HTML
New Product Submission Checklist - Export Only Additional Information 2013-11-18 HTML
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