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Autor:
Assena H. Stoimenova, Bogdan J. Kirilov, Stanislav R. Gueorguiev, Elina S. Petkova-Gueorguieva, Sava G. Ognianov
Publikováno v:
Folia Medica, Vol 62, Iss 1, Pp 165-171 (2020)
Background: The manufacture of medicinal products for human use in the European Economic Area is governed by European Directives and Regulations stipulating the relevant principles and guidelines of Good Manufacturing Practice, describing the minimum
Externí odkaz:
https://doaj.org/article/753dd7d206c64685a098428b8ed0b482
