Capillary Electrophoresis System Optimizes IgG Purity Analysis
The advanced capillary electrophoresis system, Maurice, from ProteinSimple is used for the quantitative analysis of identity, purity, and heterogeneity profiles of biopharmaceuticals. The system includes a native fluorescence detection mode, capability for size-based separation across a broad range of molecules, and offers optimized methods for IgG purity analysis. Maurice includes a cartridge for each application, which allows researchers to swap between applications without cleanup steps or a risk of cross-contamination. The platform includes three systems: Maurice C. for quantitative pI and Charge heterogeneity analysis, Maurice S. for IgG purity analysis by CE-SDS, and Maurice which completes both applications.
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Current Issue
USP Proposes a New Chapter for Rapid Sterility Testing
The US Pharmacopeial Convention (USP) is developing a new chapter for rapid sterility testing of short-life products based on the recommendations of a panel of experts and stakeholders.
Study on an Inactivation Evaluation Method of Cleaning Processes for Biopharmaceuticals
This study was successful in establishing a reliable and effective method for evaluating cleaning processes based on risk.
Ensuring Viral Safety of Viral Vaccines and Vectors
Viral vaccines and viral vectors used in biotherapeutic applications carry the risk of microbial contamination, which must be addressed.
Outsourcing
BeiGene Selects GE Healthcare’s Biologics Factory to Boost its Manufacturing Capacity
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Biopharma Demand Continues to Influence CMO Actions
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Be a Part of the Solution
Sharing of bioprocessing know-how can help resolve pressing industry problems.
SGS Increases Biopharma Characterization Capabilities
An expansion of laboratory facilities in Geneva, Switzerland expands SGS services for high-order structure analysis.
Standards/Regulations
USP Proposes a New Chapter for Rapid Sterility Testing
The US Pharmacopeial Convention (USP) is developing a new chapter for rapid sterility testing of short-life products based on the recommendations of a panel of experts and stakeholders.
Study on an Inactivation Evaluation Method of Cleaning Processes for Biopharmaceuticals
This study was successful in establishing a reliable and effective method for evaluating cleaning processes based on risk.
PDA’s New Technical Report Highlights Data Integrity Management System for Pharma Labs
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