Webinar presentation from Karen Wolfrom, Global Head of Regulatory, Cell & Gene Technologies on the latest and most important regulatory considerations in the pathway to commercialization of cell & gene therapy products
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Micro-dosing – Powder in Capsule Technology Pathway from Development to Commercialization
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The Early Advantage for IND Success and Beyond
Many of the decisions made during the early days of building and compiling the manufacturing...
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Q&A: Why Use GS piggyBac® Transposase Technology for Expression of Your Biotherapeutics?
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Whatever proves the best option, the talented Lonza team has the skills to identify it, and then...
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Optimizing GMP Manufacturing of Lipid Nanoparticles
Lonza is now offering next-generation encapsulation of nucleic acids with FDmiX. In this...
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Simplify the encapsulation process of nucleic acid payloads with FDmiX technology
Enable a reliable, swift scale-up to cGMP manufacturing for mRNA encapsulation with the high-end...
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Q&A: How to Maximise Cell Line Productivity and Efficiency
In this interview, Dr. Tabitha Bullock, a principal group leader at Lonza, tells us about some...
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Lonza Bend Capabilities
At Lonza's facility in Bend (OR), our core capabilities include bioavailability enhancement,...