On-Demand Webinars
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T3P – A Green Solution For Peptide Coupling, Water Removal Reactions
1/13/2026
The session focuses on the use of T3P (propanephosphonic acid anhydride) in amidation and peptide coupling reactions, including both liquid-phase and solid-phase peptide synthesis.
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Reimagining API Manufacturing – How To Achieve Smarter, Scalable Flow Chemistry
1/13/2026
Designed for scientists and engineers evaluating advanced reactors, this recording delivers practical insights and real-world examples to support safer, more efficient, and adaptable flow chemistry.
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Enhancing Automated Environmental Monitoring In Gloveless Isolators
1/7/2026
Explore how automation and robotic-friendly solutions are transforming fill-and-finish operations and gain insights into gloveless processes, EM testing challenges, and collaborative innovations.
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The Impact Of PEGs In The Small Molecule API Market
12/22/2025
Explore how PEG selection shapes drug development success by understanding the benefits of expert CDMO partnerships that deliver custom solutions to enhance your small molecule program.
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Five Practical Considerations To Move From Concept To Clinic
12/17/2025
Learn more about five key factors for advancing targeted in vivo LNP programs, from formulation and targeting strategies to bioanalytical readiness and scalability.
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Agile Adaptation In mRNA-LNP Manufacturing: A CDMO's Response
12/17/2025
Find flexible scale-up from lab through commercial manufacturing, leveraging expertise. Gain technical insights for scalable, efficient development for advancing mRNA, saRNA, or circular RNA programs.
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Hear From The Experts: LNPs Driving The Future Of Cell Therapy
12/12/2025
Explore how lipid nanoparticles are driving breakthroughs in cell therapy, from mRNA-based immune cell engineering to genome editing for CAR T cells and HSPCs from leading experts.
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Manufacturing Made More Robust And Customer-Centric
12/11/2025
Discover how regional manufacturing, risk-aware practices, and agile strategies are reshaping supply chains to deliver resilience, transparency, and sustainability in today’s complex global environment.
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Eliminate Risk From Your Viral Vector Tech Transfers
12/5/2025
Explore strategies to simplify viral vector tech transfers, reduce risk, and maintain quality under tight timelines, as well as a case study that demonstrates how to streamline this critical process.
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Navigating Regulatory Expectations For Injectable Packaging
12/4/2025
Explore insights on extractables, focusing on how they relate to the revised EU GMP Annex 1, new and evolved expectations under USP <382>, and the use of VHP decontamination in aseptic environments.