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

Abstract

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.

Keywords

• regulation (eu) 2019/6
• legislation
• commercialization
• veterinary drug