This guide shows the additional requirements that you need to be aware of when supplying POM-V or POM-VPS products …
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it might be better to transfer the drug in question to the clinic itself and then allow them to dispense as appropriate. In general, veterinarians must charge adequately for their professional services to cover the costs of maintaining a veterinary clinic, paying staff, and offering quality medical care to a client’s animal. Group 1 â Legislation pertaining to veterinary biologics, Group 3 â Guidelines and information on veterinary biologics, Canadian Food Inspection Agency Fees Notice, CFIA/ACIA 4720 – Application for Services, CFIA/ACIA 1493 – Application for Permit to Import Veterinary Biologics into Canada, CFIA/ACIA 1503 – Veterinary Biologic Information, CFIA/ACIA 2205 – Notification of Suspected Adverse Events to Veterinary Biologics, CFIA/ACIA 5761 – Canadian Centre for Veterinary Biologics (CCVB) – Product Label Submission, CFIA/ACIA 5212 – Revisions to Outlines of Production and Special Outlines for Veterinary Biologics (Licensed in the United States), CFIA/ACIA 5213 – Application for the Renewal of Product Licensing and Renewal of Import Permits for Licensed Veterinary Biologics Manufactured in the, CFIA/ACIA 5214 – Application for Renewal of Veterinary Biologics Establishment Licence and Product Licence, CFIA/ACIA 5569 – Information Required for Autogenous Veterinary Biologics, Manufacturer's Serial Release Test Report, Guidance for Preparation of New Product Licensing (Registration) Submissions for Veterinary Biologics, Guideline for Regulation of Biotechnology-Derived Veterinary Biologics, Guideline for Labelling of Veterinary Biologics, Guideline for Pre-Submission Consultation Meetings and Advance Notification of New Product Licensing Submissions, Guideline for Advertising of Veterinary Biologics, Guideline for Bluetongue Virus Exclusion Testing of Veterinary Biologics, Guideline for Preparation of Production Outlines, Special Outlines, and Summary of Changes for Veterinary Biologics, Guideline for Inspection of Veterinary Biologics Manufacturers and Importers, Guideline for Autogenous Veterinary Biologics, Guideline for Reporting Suspected Adverse Events Related to Veterinary Biologics, Guideline for Registration of Immunoglobulin Supplements, Guideline for Reporting Laboratory and Field Efficacy Trials, Guideline for Licensing Veterinary Diagnostic Test Kits in Canada, Guideline for the Importation and/or Release of Unlicensed Veterinary Biologics for Research or Emergency Use, Guideline for the Release of Unlicensed Veterinary Biologics Manufactured in Canada, Guideline for the Importation of Unlicensed Veterinary Biologics Manufactured in a Foreign Country, Requirements for master seed stocks, master cell stocks and veterinary biologic serials, Guideline for Licensing Veterinary Nucleic Acid Vaccines, Guideline for Inspection of Veterinary Biologics Importers, Guideline for Issuance of Veterinary Biologics Export Certificates, Guideline for Safety Requirements for Veterinary Biologics, Guideline for Pseudorabies Virus Exclusion Testing of Veterinary Biologics, Guideline for minimising the risk of introducing transmissible spongiform encephalopathy prions and other infectious agents through veterinary biologics, Guideline for Commercial Importers of Veterinary Biologics in Canada, Guideline on Facility Requirements for Veterinary Biologics, Veterinary Biologics Program Service Standards (Response Times), Licensing Requirements for Veterinary Biologics – Overview, The Regulation of Veterinary Biologics in Canada – Overview, Importation of Veterinary Biologics – Overview, The Canadian Biosafety Standards and Guidelines, Canadian Council on Animal Care (CCAC) Guidelines, Codes of Practice for Care of Farm Animals, Harmonization of Technical Requirements for Registration of Veterinary Medicinal Products (VICH).