ArticlesBioPharma July 13, 2023 Pulling Out All the Stops in mAb Manufacturing While the biopharma industry is pushing the barriers with antibody development, it must also contend… admin-element
ArticlesDownstream June 13, 2023 Pushing the Barriers in Next-Gen Antibody Development Continued development of new and next-generation antibodies is spurred by the increasing demand for more… admin-element
ArticlesDownstream May 19, 2023 eBook: Purification of Antibody Therapeutics – Approach for Diversified Pipeline Antibody therapeutics are the largest class of biotherapeutics. Over the years, development... admin-element
ArticlesUpstream October 21, 2021 Cell Culture Media Selection Guide for Your Lab Wall Doing cell culture and upstream process development on antibodies, vaccines, or viruses? admin-element
ArticlesDownstreamRegulatoryUpstream November 5, 2020 Reimagining Affordable Biosimilars Drug development is undergoing a transformation from multi-billion-dollar blockbusters to personalized... admin-element
ArticlesBioPharmaDownstreamUpstream January 31, 2019 Modeling the Degradation of mAb Therapeutics Ensuring the stability of biotherapeutic products, which has an impact on their safety and... admin-element
ArticlesBioPharmaRegulatory July 18, 2014 Defining Critical Quality Attributes for Monoclonal Antibody Therapeutic Products A critical quality attribute (CQA) has been defined as “a physical, chemical, biological... admin-element