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- W3048004820 abstract "The article is focused on studying the specifics of legal regulation of state supervision in the field of retail trade in medicinal products. The essence of state supervision and retail trade in medicinal products has been revealed. The author has emphasized on specific features of regulatory principles for retail trade in medicinal products. The system of regulatory acts regulating the procedure of state supervision in the field of retail trade in medicinal products has been outlined. The powers of state supervisory agencies in regard to conducting scheduled and unscheduled inspections of pharmacies have been studied. The grounds and procedure for conducting such inspections have been determined. The author has provided the requirements of the licensing conditions for a pharmacy that accomplishes retail trade in medicinal products. The subject matter of state supervision in the field of retail trade in medicinal products has been determined. The own definition of the state supervision in the field of retail trade in medicinal products has been offered. The specific features of the implementation of control and supervision measures in the field of retail trade in medicinal products have been defined. It has been emphasized that the peculiarities of state supervision in the field of retail trade in medicinal products are the specific subject matter of such a supervision, the presence of a special agency authorized to conduct inspections of the compliance with the legislation in this area. It has been established that the implementation of state supervision is possible with the presence of special knowledge not only in the field of jurisprudence, but also in the pharmacy area and laboratory research of medicinal products' quality. It has been noted that the regulation of state supervision in the field of retail trade in medicinal products includes a wide range of regulations that contain the system of homogeneous social relations regulating pharmaceutical activities through sub-institutions of the circulation of medicinal products, which are the creation, production, storage, transportation, control over the quality, import, export, sale and disposal of medicinal products." @default.
- W3048004820 created "2020-08-13" @default.
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- W3048004820 date "2020-01-01" @default.
- W3048004820 modified "2023-10-16" @default.
- W3048004820 title "Правове регулювання державного нагляду у сфері роздрібної торгівлі лікарськими засобами" @default.
- W3048004820 doi "https://doi.org/10.32837/yuv.v0i1.1569" @default.
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