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pro vyhledávání: '"Aynur Ozel Babacanoglu"'
Publikováno v:
Acta Poloniae Pharmaceutica, Vol 81, Iss 2, Pp 279-286 (2024)
Elemental impurities contained in drug product create a risk for patients and potential toxic elemental impurities defined and classified in Guideline for Elemental Impurities Q3D(R1). Among the finished product dosage forms, parenteral products coul
Externí odkaz:
https://doaj.org/article/a113bd8cbd644488a5d00716fee0d858