Incorporating regulatory requirements into the product life cycle is crucial.
This article explores lab data integrity violation trends, as well as a sampling of the latest technologies that can help avoid them.
The authors review how media components modulate the quality of monoclonal antibody products
The authors review how media components modulate the quality of monoclonal antibody products
Protecting against microbiological contaminationover the whole manufacturing process grows increasingly important.
A case study to compare the performances of several types of mixing in disposable bags with stainless steel bioreactors.
The authors review methods for generating monoclonal antibodies for research and development.
The authors review methods for generating monoclonal antibodies for research and development.
The authors review methods for generating monoclonal antibodies for research and development.
The authors review methods for generating monoclonal antibodies for research and development.
The authors review methods for generating monoclonal antibodies for research and development.
The authors review methods for generating monoclonal antibodies for research and development.
Dr. Grabski discusses why MCC offers significant economic advantages over traditional batch chromatography methods for purification of monoclonal antibodies. Live: Tuesday, Nov. 19, 2019 at 11am EST | 8am PST | 4pm GMT | 5pm CET Register free
The authors give special consideration factors affecting blow–fill–seal technology.
Webinar Date/Time: Tue, May 2, 2023 11:00 AM EDT
Proposed changes to rules governing the commercialization of technologies developed with federal funding prompts significant stakeholder feedback.
Using cholesterol-modified oligonucleotides, the research team aims to improve the delivery of antisense nucleotide-based therapies for treating neurodegenerative diseases and brain cancers.
Consider automation early in the rollout of clinical translation and scale up of clinical-trial protocols.
Consider automation early in the rollout of clinical translation and scale up of clinical-trial protocols.
Consider automation early in the rollout of clinical translation and scale up of clinical-trial protocols.
Hydrophobic interaction chromatography (HIC) in flow-through mode offers a more efficient and cost-effective polishing/purification process to remove monoclonal antibody aggregates while maintaining purity at ≥99% than a mixed-mode bind/elute procedure.
A case study demonstrates that affinity chromatography can offer efficiency and scalability for gene therapy manufacturing using viral vectors.
A case study demonstrates that affinity chromatography can offer efficiency and scalability for gene therapy manufacturing using viral vectors.
A case study demonstrates that affinity chromatography can offer efficiency and scalability for gene therapy manufacturing using viral vectors.
Using a hollow microstructured transdermal system to deliver vaccine directly to the dermis.