Lv11
96 积分 2024-05-09 加入
〈1207〉 Package Integrity Evaluation—Sterile Products
39分钟前
求助中
High concentration formulation developability approaches and considerations
6个月前
已完结
Simultaneous Analysis of the Drug-to-Antibody Ratio, Free-Drug-Related Impurities, and Purity of Antibody–Drug Conjugates Based on Size Exclusion Chromatography
7个月前
已完结
Extending the limits of size exclusion chromatography: Simultaneous separation of free payloads and related species from antibody drug conjugates and their aggregates
7个月前
已完结
Analytical Quality by Design as applied to the development of a SEC-HPLC platform procedure for the determination of monoclonal antibody purity without mobile phase additives
7个月前
已完结
Accelerated development of a SEC-HPLC procedure for purity analysis of monoclonal antibodies using design of experiments
7个月前
已完结
Accelerated development of a SEC-HPLC procedure for purity analysis of monoclonal antibodies using design of experiments
7个月前
已完结
Modifying insulin to improve performance
9个月前
已完结
Quantitation of activated factor VII levels in plasma using a tissue factor mutant selectively deficient in promoting factor VII activation
9个月前
已完结
Enzymatic removal of sialic acid enables iCIEF stability monitoring of charge variants of a highly sialylated bispecific antibody
10个月前
已完结
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