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 Implementing a Quality by Design (QBD) Approach In Integrated DSP In-Line PAT... Dejan Arzenšek, at Novartis and Justin Moretto at Kaiser Optical Systems, Inc. Full Title: Implementing a Quality by Design (QBD) Approach In Integrated DSP In-Line PAT Advanced Analytical Technologies to Monitor Critical Quality... 9 months ago | 117 mins Process Analytical Technologies – Advances in Bioprocess Integration... Marina Kirkitadze at Sanofi Pasteur and Gabriella Gerzon, PhD Candidate, York University, Toronto, Canada Full title: Process Analytical Technologies – Advances in Bioprocess Integration to Transition to Digital Manufacturing Process Analytical Technology... January 25, 2023 3:00pm Integrity Assurance for Single-Use Systems: End-User Perspective Charlotte Masy at GSK Vaccines and Patrick Evrard at Pall Life Sciences Single-use technologies are more and more used in critical sterile applications, e.g. close to final manufacturing steps handling Drug Product, leadin... 8 months ago | 126 mins Utilizing Cell Culture Platform and High-Throughput Bioreactors to Streamline... Sanjeev Gupta, Ph.D., Vice President and Head Advanced Biotech (Biosimilar Division), Ipca Laboratories Ltd., Mumbai-India Full title: Utilizing Cell Culture Platform and High-Throughput Bioreactors to Streamline Upstream Process Development and manufacturing scale up Di... November 15, 2022 9:00am Quality-By-Design in Spray Drying Processes - Transfer Lab to Production Sune Klint Andersen, Janssen Pharmaceutica & João Vicente Senior Scientist - Particle Engineering Team Leader at Hovione Spray drying is a continuous and scalable manufacturing process commonly used in the pharmaceutical industry. Due to its scalable and continuous natur... 3 years ago | 77 mins From Early Stage to Late Stage Development: How to Characterize a Perfusion-base Perrine Rouel, Janssen Pharmaceutical Companies of Johnson & Johnson and Tom Jeffery, Sartorius Stedim Biotech Full Title: From Early Stage to Late Stage Development: How to Characterize a Perfusion-based Vaccine Production Process Using QbD? The biopharmaceut... 3 years ago | 58 mins Facilitating CMC Development and Regulatory Filings with Phase-Appropriate QbD Tiffany Rau, PhD, Rau Consulting LLC, Phil Ramsey, PhD, Predictum Inc., and Wayne Levin, Predictum Inc. Pharmaceutical and biotechnology companies are under increasing pressure to reduce timelines and costs to speed up the delivery of safe and high-quali... 2 years ago | 54 mins Biopharmaceutical process development – Trends/ Challenges/Opportunities Kumar Gaurav, AGM (Regulatory Affairs) at Panacea Biotec Ltd and Sudhakar Nagaraj, Principal Scientist, SLS at Pall Biotech Presented by Kumar Gaurav, AGM (Regulatory Affairs) at Panacea Biotec Ltd Current trends and regulation affecting Biopharmaceutical Industry Journey ... 2 years ago | 63 mins Innovative solutions from Industry 4.0 Michael May, President and CEO, CCRM at Centre For Commercialization Of Regenerative Medicine and Philip G. Vanek of GE -Potential to providing real-time visibility -Control across complex cell and gene therapy supply chains -QbD -How can industry 4.0 drive the industry... 3 years ago | 75 mins Applying Low Frequency Raman to QbD in Pharmaceutical Development John Wasylyk, Senior Principal Scientist at Bristol-Myers Squibb and James Carriere, Product Line Manager at Coherent Low frequency Raman spectroscopy has been used to study various polymorphs and can be applied to the design of crystallization control strategy. Exten... 3 years ago | 65 mins
