Pharmacovigilance

Guidance on Pharmacovigilance reporting.

  1. The wholesale dealer must supply information and samples to the Secretary of State on demand.

  2. If the wholesale dealer is notified of an adverse event to a veterinary medicinal product that they have supplied, then further checks must be made to ensure that the adverse event has been reported to the marketing authorisation holder. If the adverse event has yet to be reported, then the wholesale dealer must direct the person to report it directly to the marketing authorisation holder.