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Advice on product information of veterinary medicines

Directive 2001/82/EC, as amended, provides for that the product information of a veterinary medicinal product is appropriately reported in the Summary of Product Characteristics (SmPC), Patient Information Leaflet (PIL) and labelling. Maximum care is therefore required in the drafting of these documents, that are integral part of the authorisation dossier.

The main services offered in this field are:

  • translation and update of the SmPCs, labelling and information leaflets.
  • preparation of artworks for the immediate and secondary packaging and for the patient leaflet
  • pharmaceutical packaging graphic design
  • review of advertising messages and Ministry procedure for the authorisation application of non-prescription veterinary medicines

Foto di: mbfrye da Pixabay