Commercial-scale viral vector manufacture: technical challenges & strategic implications
On demand

Commercial-scale viral vector manufacture: technical challenges & strategic implications

Wednesday 08:00 PST / 11:00 EST / 16:00 GMT / 17:00 CET
Commercial-scale viral vector manufacture: technical challenges & strategic implications

Following recent mainstream media coverage of reported supply and demand mismatch, viral vectors now dominate much of the discussion within the cell and gene therapy sector. This On Demand panel webinar provides insight from three leading experts at the forefront of vector manufacturing, as they share their first-hand experiences in moving to commercial-scale manufacture of viral vectors including:

  • Current approaches to commercial-scale manufacture of viral vectors and the unique challenges/limitations of each.
  • Real world experience of the different upstream and downstream processes and their impact on yield, efficiency, safety, cost of goods.
  • Potential impact of vector manufacturing decisions on your business model and clinical development timeline.

Hear from our panel of industry experts:

  • Dr Michael Kelly, Director, Asset Leadership, Gene Therapy, Biogen
  • Dr Clive Glover, Senior Global Marketing Manager, Cell & Gene Therapy, Pall Life Sciences
  • Dr Richard Snyder, Chief Scientific Officer, Brammer Bio

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Michael Kelly
Michael Kelly
Director, Asset Leadership, Gene Therapy at Biogen Idec
Dr. Mike Kelly has over 20 years of experience in the field of gene therapy. During this time, Mike has been responsible for various aspects of research, development and clinical manufacturing for a number of lentiviral, adenoviral and Adeno-associated virus (AAV) -based therapeutics. Currently, Mike works at Biogen, where he is a Director in the Asset Development and Portfolio Management group, leading the gene therapy portfolio. Prior to his current role, Mike was the Director of Gene Therapy Development at Genzyme Corporation, where he was responsible for process development and manufacturing for Genzyme’s gene therapy programs. Prior to that, Mike was most recently the Site Director at Genzyme’s development and clinical manufacturing facility in San Diego. Before joining Genzyme, Mike worked at Cell Genesys and Somatix Therapy Corporation, where he held various roles in research and development and clinical manufacturing for gene therapy programs.
Clive Glover
Clive Glover
Director, Strategy at Pall Biotech
Dr Clive Glover is the Director, Strategy at Pall Biotech where he leads Pall’s cell and gene therapy business. Previously he was responsible for driving product development efforts around cell therapy at GE Healthcare and has also held positions in marketing and product management at STEMCELL Technologies. Clive holds a PhD in Genetics from the University of British Columbia.
Richard Snyder
Richard Snyder
CSO at Thermo Fisher Scientific

Richard O. Snyder, PhD is the Vice President for Science and Technology, Pharma Services, Viral Vector Services at Thermo Fisher Scientific. Dr. Snyder has been investigating virus biology, vector development, cGMP vector manufacturing and analytical technologies, and viral vector-mediated gene transfer for over 33 years, and was a member of teams who developed novel viral vector-based human gene therapies.

Dr. Snyder was an Associate Professor of Molecular Genetics and Microbiology, and Director of Biotherapeutic Programs at the University of Florida; an Assistant Professor of Pediatrics at Harvard Medical School; and was previously employed by Cell Genesys, Somatix, Merlin, and Avigen where he was engaged in the development of gene transfer vector and vaccine technology, along with therapeutic applications. Dr. Snyder was a postdoctoral fellow at Johns Hopkins University School of Medicine, received his doctoral degree in Microbiology from The State University of New York at Stony Brook, and obtained his B.A. in Biology from Washington University in St. Louis.