Zobrazeno 1 - 3
of 3
pro vyhledávání: '"S. A. Manaeva"'
Autor:
Yu. V. Olefir, T. N. Bokovikova, L. A. Stronova, E. P. Gernikova, L. I. Mitkina, S. A. Manaeva, Yu. B. Purim, A. V. Pichugin
Publikováno v:
Регуляторные исследования и экспертиза лекарственных средств, Vol 0, Iss 1, Pp 37-40 (2018)
The present article describes the approaches to the choice of methods for assessing the content of visible particles in parenteral and ophthalmic dosage forms, recognized in general pharmacopoeia monograph «Visible particles in parenteral dosage for
Externí odkaz:
https://doaj.org/article/852ab8590c7b4212aefc7687e03b7ab1
Autor:
T. N. Bokovikova, E. P. Gernikova, E. I. Sakanyan, N. D. Bunyatyan, L. I. Shishova, L. A. Stronova, S. A. Manaeva
Publikováno v:
Регуляторные исследования и экспертиза лекарственных средств, Vol 0, Iss 1, Pp 33-36 (2018)
Sampling procedure is an integral part of the drug quality control system. Objective science-based sampling is an important operation when only a small amount of a material is taken and it is representative for the analysis of the whole product batch
Externí odkaz:
https://doaj.org/article/db357e0373e84c61b1051fad76d9e514
Autor:
O. A. Baturina, E. V. Chaykovskaya, E. P. Gernikova, T. N. Bokovikova, L. A. Stronova, Yu. R. Biglova, S. A. Manaeva, E. S. Tolmacheva
Publikováno v:
Регуляторные исследования и экспертиза лекарственных средств, Vol 7, Iss 3, Pp 164-169 (2018)
The article summarizes the results of information analysis of bisoprolol fumarate synthesis methods which differ in the number of stages and in raw materials used, and are associated with the major identified impurities A, E and G, according to the E
Externí odkaz:
https://doaj.org/article/91c8f33969ae4708ae78211ec177e7c1