Implications of the new Regulation (U.E.) 2019/6 on veterinary medicinal products in the activity of practicing veterinarians

This material is intended to convey the main elements of Regulation (EU) 2019/6 of the European Parliament and of the Council of 11.12.2018 on veterinary medicinal products and repealing Directive 2001/82 / EC. The needs of the veterinary sector differ substantially from those of the human sector in...

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Main Author: Romeo Teodor Cristina
Format: Article
Language:English
Published: Romanian National Association of the Veterinary Products Manufacturers 2021-06-01
Series:Medicamentul Veterinar
Subjects:
Online Access:http://www.veterinarypharmacon.com/docs/2285-2021_VD_15(1)_ART.2.ROM.pdf
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author Romeo Teodor Cristina
author_facet Romeo Teodor Cristina
author_sort Romeo Teodor Cristina
collection DOAJ
description This material is intended to convey the main elements of Regulation (EU) 2019/6 of the European Parliament and of the Council of 11.12.2018 on veterinary medicinal products and repealing Directive 2001/82 / EC. The needs of the veterinary sector differ substantially from those of the human sector in terms of medicines. This U.E. lays down rules for: manufacture, placing on the market, import, export, making available, distribution, pharmacovigilance, control and use of veterinary medicinal products. The main issues covered were: sale: wholesale, retail and online, use of veterinary medicinal products, veterinary prescription and records, waiting period for a.u.v. products, advertising and controls in light of the new regulations.
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spelling doaj.art-f97e1946748a4215941eb5972ae981442022-12-21T22:32:01ZengRomanian National Association of the Veterinary Products ManufacturersMedicamentul Veterinar1843-95272069-24632021-06-01151420Implications of the new Regulation (U.E.) 2019/6 on veterinary medicinal products in the activity of practicing veterinariansRomeo Teodor Cristina0https://orcid.org/0000-0002-5420-1516Faculty of Veterinary Medicine TimisoaraThis material is intended to convey the main elements of Regulation (EU) 2019/6 of the European Parliament and of the Council of 11.12.2018 on veterinary medicinal products and repealing Directive 2001/82 / EC. The needs of the veterinary sector differ substantially from those of the human sector in terms of medicines. This U.E. lays down rules for: manufacture, placing on the market, import, export, making available, distribution, pharmacovigilance, control and use of veterinary medicinal products. The main issues covered were: sale: wholesale, retail and online, use of veterinary medicinal products, veterinary prescription and records, waiting period for a.u.v. products, advertising and controls in light of the new regulations.http://www.veterinarypharmacon.com/docs/2285-2021_VD_15(1)_ART.2.ROM.pdfregulation (eu) 2019/6legislationcommercializationveterinary drug
spellingShingle Romeo Teodor Cristina
Implications of the new Regulation (U.E.) 2019/6 on veterinary medicinal products in the activity of practicing veterinarians
Medicamentul Veterinar
regulation (eu) 2019/6
legislation
commercialization
veterinary drug
title Implications of the new Regulation (U.E.) 2019/6 on veterinary medicinal products in the activity of practicing veterinarians
title_full Implications of the new Regulation (U.E.) 2019/6 on veterinary medicinal products in the activity of practicing veterinarians
title_fullStr Implications of the new Regulation (U.E.) 2019/6 on veterinary medicinal products in the activity of practicing veterinarians
title_full_unstemmed Implications of the new Regulation (U.E.) 2019/6 on veterinary medicinal products in the activity of practicing veterinarians
title_short Implications of the new Regulation (U.E.) 2019/6 on veterinary medicinal products in the activity of practicing veterinarians
title_sort implications of the new regulation u e 2019 6 on veterinary medicinal products in the activity of practicing veterinarians
topic regulation (eu) 2019/6
legislation
commercialization
veterinary drug
url http://www.veterinarypharmacon.com/docs/2285-2021_VD_15(1)_ART.2.ROM.pdf
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