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Written by Administrator   

In this part the guidance documents for reporting of adverse reaction of other non-medicinal products regulated by ÚSKVBL are provided. The guidance cover veterinary preparations and veterinary technical devices. The report can be sent by its manufacturer, wholesaler, holder of approval, user or person performing technical check in case of veterianry technical devices. In this chapter the relevant forms are available.

Last Updated on Monday, 14 May 2018 13:10