The Canadian representative is responsible for the quality of VHPs sold in Canada and has systems in place to take corrective actions on time for all products if needed. Corrective action is required because those Veterinary Health Products that do not meet VHP requirements and relevant regulatory provisions are considered by Health Canada to be unsafe. The agency deems that these products cause the public to be deceived. Responsibilities of a VHP Canadian Representative include:
- Implementing collection of sales data for each product in the case of a product recall
- Verifying the safety of the product
- Collecting all adverse event reactions data
- Reporting severe adverse event reactions
- Attesting the use of GMP in manufacturing, labeling, packaging, distribution, and sale of the product
Moreover, the Canadian Representative has ‘read access’ to the VHP Notification Form that is submitted to Health Canada. To ensure that their responsibilities and obligations are successfully met, an agreement takes place between the Canadian Representative and the product sponsor.
- Implementing collection of sales data for each product in the case of a product recall
- Verifying the safety of the product
- Collecting all inimical event reactions data
- Reporting severe adverse event reactions
- Attesting the use of GMP in manufacturing, labeling, packaging, distribution, and sale of the product
Moreover, Canadian Representative has ‘read access’ to the Notification Form. To ensure that their responsibilities and obligations are successfully met, an agreement takes place between the Canadian Representative and the product sponsor.