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Publikováno v:
Ведомости Научного центра экспертизы средств медицинского применения, Vol 13, Iss 1, Pp 77-88 (2023)
Russian and international regulatory documents require that analytical procedures for establishing bioequivalence and comparability of quality attributes of biotechnological (biological) products, carrying out batch release of medicinal products, and
Externí odkaz:
https://doaj.org/article/d6fd7359d73b4bbc8d3817c970259007