- Memorandum 2024-01: Renewal of veterinary biologics establishment licences, product licences, and import permits
- Memorandum 2022-01: Criteria to waive laboratory animal batch safety testing for veterinary vaccines
- Memorandum 2018-05: Requirements for submission of United States Department of Agriculture (USDA) digitally signed outlines of production and special outlines of veterinary biologics
- Memorandum 2018-04: Mandatory bilingual labelling of veterinary biologics
- Memorandum 2018-03: Senecavirus A as a potential contaminant of swine origin raw materials and seed stock used in the production of veterinary biologics
- Memorandum 2018-02: Criteria to waive target animal batch safety testing for veterinary vaccines
- Memorandum 2017-04: Submission of French-language product compilation summaries for posting on the USDA website
- Memorandum 2017-03: Accommodation of US single-tier labels
- Memorandum 2017-02: Results of serial release testing of veterinary biologics imported from the US
- Memorandum 2016-02: Amendments to the nomenclature appended to the international convention the Harmonized Commodity Description and Coding System (Changes in HS codes)
- Memorandum 2013-03: Bilingual labelling of veterinary biologics
- Memorandum 2013-02: Canadian Centre for Veterinary Biologics (CCVB), Canadian Food Inspection Agency (CFIA) position statement on the extra-label use of veterinary vaccines
- Memorandum 2011-02: Harmonized data requirements for live attenuated Newcastle Disease virus vaccine master seed viruses – Intracerebral pathogenicity index testing
- Memorandum 2010-04: Requirement to test veterinary biologics for residual formaldehyde
- Memorandum 2010-03: Growth promotion testing of culture media used in quality control of veterinary biologics
- Memorandum 2010-01: Veterinary Biologics Section name change to "Canadian Centre for Veterinary Biologics"