Zobrazeno 1 - 4
of 4
pro vyhledávání: '"A. P. Meshkovski"'
Autor:
Zh. I. Aladysheva, N. V. Pyatigorskaya, V. V. Beregovykh, G. E. Brkich, A. P. Meshkovskiy, M. M. Marshalova, V. V. Belyaev, N. S. Nikolenko, E. I. Nesterkina, A. A. Kamaletdinova, M. F. Lutfullin
Publikováno v:
Регуляторные исследования и экспертиза лекарственных средств, Vol 13, Iss 3, Pp 453-463 (2023)
Scientific relevance. In December 2020, the Russian Federation adopted the Eurasian Economic Union (EAEU) requirements. This has significantly changed the certification procedure for qualified persons (QPs) of manufacturers of medicinal products for
Externí odkaz:
https://doaj.org/article/a3e0132b54024531a876bad9a6c3ceed
Publikováno v:
Acta Biomedica Scientifica, Vol 0, Iss 1, Pp 139-142 (2012)
Key competences required for any graduated specialist in the manufacture of medicines include understanding of GMP principles, good knowledge of production processes and. managerial skills. In the present day Russian Pharma Industry there is a shorta
Externí odkaz:
https://doaj.org/article/38902a7ad39a468fb84df637b36bacdd
Autor:
A. P. Meshkovskiy, V. V. Beregovykh, V. N. Shestakov, N. V. Pyatigorskaya, Zh. I. Aladysheva, N. S. Nikolenko, A. M. Pyatigorskiy, E. I. Nesterkina
Publikováno v:
Разработка и регистрация лекарственных средств, Vol 10, Iss 3, Pp 138-146 (2021)
Introduction. The article discusses significant changes in the procedure for pharmaceutical inspection of drug manufacturers for compliance with the requirements of the rules of good manufacturing practice (GMP) of the Eurasian Economic Union (EAEU),
Externí odkaz:
https://doaj.org/article/2d0217817a3342cc80fbb8969d1fb66a
Autor:
A. P. Meshkovskiy, N. V. Pyatigorskaya, Z. I. Aladysheva, V. V. Beregovykh, A. M. Pyatigorskiy, N. S. Nikolenko, M. M. Marshalova, V. V. Belyaev
Publikováno v:
Разработка и регистрация лекарственных средств, Vol 9, Iss 4, Pp 164-170 (2020)
Introduction. The article is focused on differences in quality assurance-related obligations and responsibilities between Marketing Authorisation Holders (MAHs) and manufacturing authorisation holder (manufacturers) in pharmaceutical industry. In cas
Externí odkaz:
https://doaj.org/article/2cfb3fb55f4c42ddabecd9cf63568154