Whitepapers

Monitoring and controlling your bioprocess just got easier with simplified sample loading. Watch Ryan Lybarger, Senior Field Application Consultant, demonstrate how to analyze substrates, metabolites, product titer, and more.

Cerba Research initiated custom kit building and distribution for an infectious disease study, during the COVID-19 pandemic, in 10 days. A typical timeline is 8 weeks.

This case study will examine the subject of single-use plastics used in biopharmaceutical manufacturing and extractables & leachables from the perspective of the contract research organization.

For immuno-oncology trials, partner with a global central lab that can generate early insights to optimize your protocol and ramp up to commercial scale while preserving budgets and timelines.

A frozen shipping study conducted on single-use fluoropolymer bags following new guidelines that help to mitigate the risks during frozen shipping while ensuring consistent product quality in cold chain distribution.

Method for capture of scFV and post-capture-washing condition with chaotropic agents is described. The post-capture washing condition significantly improved HCP removal to increase scFV purity.

Glycosylation homogeneity and pattern can be increase with cell line engineering and bioprocess optimization. But, these can be time-consuming and might compromise yield. In vitro glycoengineering can solve these problems and is independent from the cell line and the bioprocess used.

Despite exhausting all disinfection methods after resuming operations this year, this international biologics provider repeatedly failed Environmental Monitoring test standards, delaying $5M in product release. See how Bioquell’s Rapid Bio Decontamination Service provided a fast, effective solution.

Bridging Anti-CHO HCP Antibodies from Two 3rd Generation Cygnus CHO HCP ELISA Kits by AAE-MS

This application note collection will help ensure you have the right tools to succeed in the biopharmaceutical environment, from research and process development to quality control.

Digital transformation in pharma is not just about going paperless. It’s using technology and data to build a scientific and business ecosystem, reducing risk, accelerating innovation, and driving growth.

See real-world examples of digital transformation – including a digitally native biomanufacturer. Learn how a harmonized digital ecosystem can transform your labs for performance, insights, and innovation.

Routine Environmental Monitoring in GMP cleanrooms is a manual process and can be complex, involving thousands of sample data points per month, manual data transcription and all too frequently data gaps and integrity challenges. This paper shows how the new MET ONE 3400+ non-viable air particle counter from Beckman Coulter Life Sciences can be automated to help manage these challenges.

Transmissible diseases are no longer scarce and geographically limited, but are becoming a frequent occurrence. To prevent the spread of outbreaks, detection and containment are the first line of defense.