Search results Search for: Search Refine your results by duration: Any Under 5 mins Under 20 mins Over 20 mins Sort by: Relevance Views Date Characterization of Residual Impurities in Gene Therapy Drug Products Jessica Townsend, at Intellia Therapeutics Eric S. Bishop, at Cygnus Technologies Characterization of residual impurities for gene therapy drug products is particularly challenging due to the complex nature of the final products as ... 3 days ago | 84 mins Orthogonal Measures of LVP Using DLS, NTA, & Micro Flow Cytometry Jim Richardson at Interius Biotherapeutics and Kevin Lance at Unchained Labs Full Title: Orthogonal Measures of Lentiviral Particle Attributes Using DLS, NTA, and Micro Flow Cytometry Orthogonal Measures of Lentiviral Particl... February 16, 2023 3:00pm Getting a Gene Therapy Product to Market: Pitfalls and How to Prevent Them Hetal Brahmbhatt, Elizabeth Simmons, Thomas Guarinoni In this webinar, industry leaders from Thermo Fisher Scientific, Viralgen, and Hemology Medicines Inc. discuss the lessons learned to get a gene thera... 2 years ago | 35 mins Enabling Scalable & Cost-Effective Point of Care for Cell & Gene Therapies Qasim Rafiq, Xavier de Mollerat du Jeu, Sean Chang The transformative potential to change the way human disease is treated using cell and gene therapy has motivated rapid technological advancements tow... 2 years ago | 62 mins Scalable AAV Manufacturing: Addressing Challenges Across the Workflow Chao Yan Liu, Gino Stolfa, Monica Commerford Thermo Fisher Scientific product experts discuss upstream and downstream solutions across the entire workflow. In this webinar, you'll learn about sc... 2 years ago | 85 mins A Successful Journey to Cell Therapy Manufacturing: From R&D to Lot-Release Kasey Kime, Sean Chang, Uma Lakshmipathy Cell therapy is a transformative cancer treatment that utilizes genetically modified cells from a healthy donor or patient's own immune system to atta... 2 years ago | 45 mins GMP Ancillary Materials for Cell & Gene Therapy Manufacturing: What to Consider Kasey Kime, Eric Roos This webinar covers regulatory requirements for GMP ancillary materials and the importance of regulatory documentation and support. Considerations for... 2 years ago | 43 mins
