Compliance and Regulations for Flow Cytometry in Drug Discovery: Webinar Series
In this webinar series, learn about 21 CFR Part 11 regulations for flow cytometry in drug discovery. Learn what software and instruments can help you comply.
Demonstrating a Modular Selectivity with a Weak AEX-HIC Resin for Achieving High mAb Purity and Recovery in a Downstream Process
Learn how Bio-Rad’s Nuvia wPrime 2A Media, a weak AEX-HIC resin, is used in an efficient monoclonal antibody (mAb) purification process. Presented by Dr. Sushmita Koley, this webcast demonstrates how multimodal chromatography improves purity and recovery, achieving a 10x reduction in high molecular weight species while maintaining 85% mAb monomer recovery. Watch to explore innovative solutions for biomanufacturing.
Evaluation of a New Multimodal Anion Exchange Resin for Emerging Biotherapeutic Process Challenges
Nuvia wPrime 2A Resin has MMAEX functionality with a weak anion exchanger. See data showing improved mAb and bsAb purification compared to traditional resins.
Cytometry in Drug Discovery: An Introduction to Regulation, Standardization, and Productivity
Many researchers learn flow cytometry in academia, but find new challenges in the commercial sector. In this webinar, learn about regulatory issues and more.
Developing Efficient Downstream Purification Processes for Bispecific Antibodies
Modern chromatographic resins enable new strategies for downstream processing of bispecific antibodies. Watch this webinar to see case studies and workflows.
How to Harness Regulatory Compliance Capabilities with Image Lab Touch Software for Western Blotting and Gel Electrophoresis
Improve western blotting and gel electrophoresis data security with Image Lab Touch Software. See features that support regulatory compliance in this webinar.
Unlocking the Potential of Cell and Gene Therapies: Overcoming Production Challenges
A common challenge in scaling up cell and gene therapy production is monitoring for contaminants, such as Mycoplasma. Learn how ddPCR can help in this webinar.
Effective Strategies for Endotoxin Removal in Therapeutic Protein Purification
Endotoxins are common impurities that pose safety risks in therapeutic protein preparations and are difficult to remove. See proven workflows and strategies.
Guidance for the Validation of qPCR and ddPCR Assays in Regulated Environments
In this webinar, learn about validating qPCR and ddPCR assays in regulated environments. Explore validation parameters and regulatory considerations.
A Polishing Strategy for Removing Impurities in Bispecific Antibody Purification
Bispecific antibodies pose unique challenges in downstream processing. See how impurities were efficiently removed by mixed-mode chromatography in this webinar.