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Legislative regulatory aspects of the veterinary pharmacy market in the European Union
Author(s) -
H. D. Harvas
Publication year - 2019
Publication title -
naukovij vìsnik lʹvìvsʹkogo nacìonalʹnogo unìversitetu veterinarnoï medicini ta bìotehnologìj ìmenì s.z. g̀žicʹkogo. serìâ ekonomìčnì nauki
Language(s) - English
Resource type - Journals
ISSN - 2519-2701
DOI - 10.32718/nvlvet-e9223
Subject(s) - european union , legislation , harmonization , legislature , pharmacy , business , animal health , pharmaceutical industry , veterinary public health , order (exchange) , public health , microbiology and biotechnology , veterinary medicine , medicine , political science , international trade , pharmacology , finance , law , physics , nursing , family medicine , acoustics , biology
Production of veterinary pharmacy plays an important role both in animal care and public health, such as for food safety or animal origin to prevent the spread of diseases transmitted to humans through animals. The European market for Animal Health develops rapidly filled with innovative products, updated regulatory system at the legislative level, in order to protect human health, animals and the environment. Today, the focus of attention in the European Union (EU) on the pharmaceutical industry – Is the improvement of the legal framework and its adaptation to the needs and characteristics of the veterinary pharmaceutical industry in particular. Thus Ukraine today - is an intensive process of harmonization, implementation and, at the same time, improvement of the regulatory system, in which international regulatory documents are the basis for the creation of the veterinary pharmaceutical legislation of Ukraine, according to EU requirements.

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