Veterinary Health Product Licensing in Ontario, Canada

VETERINARY HEALTH PRODUCT LICENSING

VHPs are low risk drugs for pet animals in certain dosage forms. They are used to maintain or promote the health and welfare of companion and food-producing animals. They are not used to treat, prevent or cure disease.

VHPs contain ingredients such as: vitamins, minerals and traditional medicines.

Companies are to notify Health Canada about their VHPs:

At least 30 days before
selling a VHP in Canada

At least 30 days before making a change to a VHP we have already been notified about in Canada

Before importing a VHP into Canada

We will facilitate the product licensing and (if necessary) ingredient approvals to get your pet-friendly products to market!

Veterinary Health Products FAQ

Do I need to register my veterinary health product (pet supplements) in Canada?

Yes, you need to register your product in Canada to receive a VHP notification number, which is a 4-digit alpha-numeric code.

Veterinary Health products need to be notified:

At least 30 days before selling a VHP for the first time in Canada
At least 30 days before making a change to a VHP that is already notified in Canada
Before importing a VHP into Canada

How long does it take to receive a Notification number in Canada?

Health Canada has a performance standard of 30 calendar days starting on filing date.

Is there a fee associated to Health Canada for a product notification?

There is a $486 CAD fee associated with product notifications or major changes to products that have been previously notified to be paid directly to Health Canada.

How do I know if my product meets the requirements for a Veterinary Health product Notification?

The product can be notified if all ingredients are listed on the permitted substances database for their given purpose (active or excipient). If an ingredient is not found on the database or indicated for the intended dosage form or for specie; then the ingredient must be added or modified on the Permitted Substances Database before proceeding with the Notification.

Do I need a Site Licence or a Certified GMP Facility to conduct manufacturing, packaging, labelling, importing, or distributing activities?

You do not need a Site Licence or a Certified GMP Facility, however you are required to follow GMP at the site and ensure that the product meets quality requirements and is not adulterated or misleading.

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