Webinars
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How A Sponsored CMC Platform Accelerates mRNA Projects Into The Clinic
1/31/2023
Developing a client-sponsored Target Product Profile (TPP) and Analytical Target Profile (ATP) is critical to move your drug product to clinic efficiently and meet acceptance criteria.
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Can A Small Plasmid Produce Huge Benefits? The Power Of Small
1/17/2023
With benefits across applications, nanoplasmids are designed to replace antiquated bacterial backbones, while eliminating antibiotic markers that can cause regulatory concerns.
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Analyzing COVID-19 Vaccine Purity Using LC-MS Technologies
11/8/2022
Explore why process-related impurities are a concern in vaccines and present results and learnings from LC-MS analyses of several mRNA- and protein-based vaccines for COVID-19.
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RNA Interference - From Single Gene Studies To Whole Genome Screens
11/7/2022
Endoribonuclease-prepared siRNAs (esiRNAs) are able to overcome the limitations of RNAi. Learn about esiRNAs, their advantages over standard siRNAs, and ways this technology is utilized in different research fields.
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The Biotech Landscape: Market Trends, Priorities, Predictions, And Pathways To FDA Approval
10/27/2022
The webinar features regulatory affairs and investment leaders from North America and Asia Pacific who will discuss why biotech companies are increasingly exploring clinical opportunities in Asia Pacific to generate diverse, globally accepted clinical trial data, and much more.
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How To Choose The Best Filtration Device For Your Application
10/6/2022
Learn how to choose the best filtration device for your specific application and understand pore size, membrane material, well volumes and tip types.
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Go/No Go Decisions Based On Early Phase Oncology Trials
9/22/2022
In this webinar, gain insight into the latest regulatory and clinical developments in the field of oncology in China.
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Development And Regulatory Strategy For US And China
9/22/2022
This webinar discusses the expansion of International Market for Ensartini and RNAi Therapeutics in Oncology, from Skin Cancers to Liver Cancers.
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Accelerating Clinical Development In China & The US
9/22/2022
Discover how the clinical research bridge between China and the US supports accelerated clinical development from early to late phase trials while ensuring the inclusion of MRCT data packages in future regulatory applications.
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A&M STABTEST Shares QC Analysis Of Oligo Therapeutics
9/20/2022
Explore best practices for developing a QC method for identification and impurity analysis of oligonucleotides, as well as tips on mitigating risk by using compliant instrumentation and software.