Lv1
18 积分 2022-05-25 加入
Pharmaceutical Forced Degradation (Stress Testing) Endpoints: A Scientific Rationale and Industry Perspective
1小时前
待确认
An Industry Perspective on the use of Forced Degradation Studies to Assess Comparability of Biopharmaceuticals
1小时前
已完结
An Industry Perspective on Forced Degradation Studies of Biopharmaceuticals: Survey Outcome and Recommendations
1小时前
已完结
Multi-attribute method for simultaneous monitoring of critical quality attributes in monoclonal antibodies: advances, challenges, and regulatory perspectives
2个月前
已完结
In-use stability of Rituximab and IVIG during intravenous infusion: Impact of peristaltic pump, IV bags, flow rate, and plastic syringes
3个月前
已完结
Comparative study between a gravity-based and peristaltic pump for intravenous infusion with respect to the generation of proteinaceous microparticles
3个月前
已完结
Current Industry Best Practice on in-use Stability and Compatibility Studies for Biological Products
5个月前
已完结
Analytical Development and Testing Strategy of Antibody–Drug Conjugates
5个月前
已完结
Current views on N-glycolylneuraminic acid in therapeutic recombinant proteins
7个月前
已完结
Effects of culture conditions on N‐glycolylneuraminic acid (Neu5Gc) content of a recombinant fusion protein produced in CHO cells
7个月前
已完结