Forms

Reporting on adverse events (TAM-Vigilance)

The duty to report adverse events to Swissmedic is specified in Article 59 of the Law on Therapeutic Products of 15 December 2000 (HMG) and in articles 35-39 of the Ordinance on Therapeutic Products of 17 October 2001 (VAM).

https://www.swissmedic.ch/content/swissmedic/en/home/tierarzneimittel/veterinary-medicines/report-adverse-drug-reaction-to-a-veterinary-medicinal-product/forms.html