Recommendations for the Contents of the “Peptide Mapping” Part of a Product Specification File

O. A. Vaganova
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Abstract

‘Identification. Peptide mapping’ is a necessary part of manufacturers’ product specification files for therapeutic proteins (active ingredients and final products of monoclonal antibodies, filgrastims, erythropoietins). The expert of the Federal State Budgetary Institution “Scientific Centre for Expert Evaluation of Medicinal Products” of the Ministry of Health of the Russian Federation provides recommendations for a step-by-step presentation of the test procedure, which will allow applicants to align product specification files for Russian- and foreign-produced medicinal products, help experts to minimise or eliminate the need to request additional information from applicants, and will contribute to timely batch release of medicinal products.
关于产品规格文件中“肽图谱”部分内容的建议
的识别。“肽图谱”是治疗性蛋白(单克隆抗体、非格昔汀、促红细胞生成素的活性成分和最终产物)生产商产品规格文件的必要部分。俄罗斯联邦卫生部联邦国家预算机构“药品专家评价科学中心”的专家为逐步介绍测试程序提供建议,这将使申请人能够调整俄罗斯和外国生产的药品的产品规格文件,帮助专家尽量减少或消除要求申请人提供额外信息的需要。并将有助于药品的及时批放行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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