This webinar will focus on best practices to navigate regulatory communications with the US FDA and how this guidance may inform pharma and biotech companies on the development of manufacturing, non-clinical development plans and investigational approaches.
Join this webinar to get insights on the US FDA guidelines and the managing of safety considerations and efficacy endpoints of these cell and gene therapy products.
Join experts from Emmes, Robert Anderson, PhD, Associate VP, Regulatory; and Kari Bingham, PharmD, CGT Safety Manager, Pharmacovigilance and Medical Monitoring, for the live webinar on Monday, October 16, 2023, at 11am EDT (4pm BST/UK).
For more information, or to register for this event, visit Cell and Gene Therapy Clinical Trials’ Regulatory Strategies and Safety Considerations.
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