Features normative legal regulation manufacture of medicines for medical and veterinary use in the light of the GMP standarts

This article presents a comparative analysis of legal regulation of drug production for veterinary use and drugs for medical use in the process of transition to the European system of rules, regulations and guidelines for the production of medicines - GMP. And also about the difficulties associated with the imperfection of the system in the current legislation. © 2018, Folium Ltd. All rights reserved.

Авторы
Deltsov A.A.1 , Kosova I.V. 2
Издательство
Общество с ограниченной ответственностью Фолиум
Номер выпуска
2
Язык
Русский
Страницы
23-27
Статус
Опубликовано
Том
10
Год
2018
Организации
  • 1 Moscow State Academy of Veterinary Medicine and Biotechnologies named K. I. Skryabin, Russian Federation
  • 2 People’s Friendship University of Russia, Russian Federation
Ключевые слова
Medicines; Pharmaceutical market; Pharmaceuticals; Pharmacy; Veterinary medicine
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/7036/
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