02.24.22 -- How To Set Up An Effective Quality Risk Management Program
02/24/22 Pharmaceutical Online Newsletter
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02/24/22 Pharmaceutical Online Newsletter
11/02/21 Pharmaceutical Online Newsletter
05.25.21 -- Are You Approaching LIMS Validation Correctly? Sanofi wanted to upgrade from an existing batch chromatography process to the BioSMB multicolumn format, then scale up that process to a continuous perfusion run. This case study details the real-world results. Featured Editorial By Tim Sandle, Ph.D., Bio Products Laboratory Ltd. Laboratory information management systems (LIMS) are an established part of larger laboratories. However, different LIMS vary in their scale, functionality, and quality. This article considers the essential validation c...
04.29.21 -- COVID-19's Impact On Outsourced Small Molecule Manufacturing Catching up to the paradigm shift in optimizing, scaling up, and manufacturing plasmids is crucial for clinical to commercial program success for gene therapies and vaccines. With an increased demand for plasmids for targeted gene therapeutic delivery, partnering with a CDMO equipped with the capacity, expertise, and equipment for plasmid DNA production is critical to ensuring a stable therapeutic supply. Join Aji Bio-Pharma to learn about methodologies to ensure effective producti...
01.28.21 -- When Pharmaceutical Automation Projects Fail: Averting Disaster Through Risk Assessment With the spread of SARS-CoV-2 (COVID-19) intensifying, scientists, together with pharmaceutical companies, are reinventing the approach of how to bring life-saving drugs to market. Attend this webinar to learn more about bringing life-saving drugs to market faster without impacting product quality, safety, or efficacy and the impacts and comparisons of classic platforms vs. new-generation platforms. And more! By Tim Sandle, Ph.D., Bio Products Laborato...