On Demand Webinars
Honeywell's Batch Historian Technology for Smarter, Faster Manufacturing Transform Your Batch Data into Actionable Insights
Pharmaceutical manufacturers often struggle with analyzing batch data due to a lack of visualization and complex reporting processes
What are the critical factors to sustain for your GMP compliance
We have developed these Five factors by looking at previous projects that we, at NSF, have worked on and by researching publicly available documents relating to remediation.
Development and Validation of a Platform Assay Method using Variable Pathlength Technology for Oligonucleotide Drug Product
This webinar will share Ionis’ experience with developing and validating a platform SoloVPE® in-process assay method for GMP manufacturing of oligonucleotide drug products.
Utilizing Nordic Hospital Data Lakes to Characterize Real-World ASCVD Populations
Cardiovascular disease (CVD) is the leading cause of morbidity and mortality worldwide, accounting for 17.9M deaths each year.
Success Factors & Best Practices for Commercial Temperature Controlled Shipments
This webinar will place an emphasis the critical successful factors in developing a GDP compliant Transportation Network
Meeting Compliance and Improving Efficiency
Audience Insights: Quality is essential for manufacturers in regulated industries, such as Life Sciences, to ensure the safety and efficacy of their products and to comply with industry regulations.
Identification of TCM Materia Medica Using FTIR
The medicinal effects of Chinese material medica (CMM) come from multicomponent compounds, so quality control methods can’t always determine the holistic fingerprints of samples.
The future of titanium dioxide in pharma
This webinar is part of ‘The future of solid dosage’, an ACG 360 webinar series covering wide-ranging, simple and transformative ways to achieve smarter pharma formulation, manufacture and packaging.
The Future of Aseptic Connections in Cell and Gene Therapies
In a market where efficiencies, cost savings, repeatable processes and safety are vital, cell and gene therapy companies must routinely evaluate their processes and analyze where improvements can be made, even down to the way they are managing fluid transfer.
Digital Transformation of Quality Management
Drive GxP compliance and operational excellence through a unified quality management approach
