By letter No Z05310-2017-OF dated 6.2.2017 Ministry of Health of the Slovak Republic requested registration holders the most frequently used categorised veterinary medicinal products, to supply medicinal products for human use included in the list of categorised medicinal products via the holder of authorisation to the large distribution of medicinal products for human use, which is also the holder of authorisation for the large distribution of veterinary medicinal products, if the holder of the marketing authorisation authorised by written authorisation.
On the invoice for the delivered medicines the supplier of the categorised medicinal product is to be the holder of the registration categorised from the holder the registration of the categorised medicinal product has been ordered.
Marketing Authorisation Holder the categorised medicinal product is contractually agreed with the holder of the authorisation; the large distribution of medicinal products for human use, which is also the holder of authorisation for wholesale distribution of veterinary medicinal products financial terms and conditions of intermediation supplies of categorised veterinary medicinal products.
This solution is consistent with the focus of Act No. 362/2011 Coll. on medicinal products and medical devices, as amended Law 306/2016 The competent authority of the Member State of origin shall notify the competent authority of the Member State of destination. responsibility for the availability of this medicine on the Slovak market The Republic in the provision of healthcare to patients and should also be Also informed about the use and consumption of the categorised product in the veterinary medicinal product care.