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Autor:
A. V. Alekhin, T. N. Erivantseva, V. V. Ryazhenov, N. N. Lyskov, N. A. Alekhina, M. M. Kuznetsova
Publikováno v:
Фармация и фармакология (Пятигорск), Vol 11, Iss 2, Pp 161-172 (2023)
The aim of the work was to study the legal aspects of the legislative regulation for manufacturing medicines in a pharmacy organization.Materials and methods. Databases of ConsultantPlus, Cyberleninka, Food and Drug Administration (FDA), European Med
Externí odkaz:
https://doaj.org/article/7457954f912b42b8adab0c2ba2fcaae5
