Förderung der Bereitstellung von Zell- und Gentherapien in der Region Asien-Pazifik
Webinar Overview
Zell- und Gentherapien bieten eine sehr effektive Behandlung unheilbarer Krankheiten und verbessern das Leben von Patienten. Während sich Biotechnologieunternehmen in der Region Asien-Pazifik somit bedeutende Möglichkeiten für Investitionen bieten, stellen sich ihnen in Bezug auf den klinischen Betrieb und den Marktzugang jedoch besondere Herausforderungen.
Join our online webinar and gain an in-depth understanding of the opportunities of cell and gene therapeutic product development and market entry strategies in this fast-evolving industry. Investigate the prospectus of operational excellence, investigator engagement, as well as patient recruitment to accelerate the journey. Additionally, explore Fortrea's solution for navigating the complexity of clinical studies in cell and gene therapy and understand the best practices in supporting the success of both emerging biotech and large pharmaceutical sponsors.
addition to the online presentations, feel free to book a seat at the actual site in Seoul, Korea, to join face-to-face discussions with Fortrea experts and key stakeholders covering the cell and gene therapy ecosystem. Share insights from various facets on advancing CGT clinical development in Asia Pacific.
Learnings
- In-depth insights towards the evolving regulatory framework for cell and gene therapy in the US as well as the major CGT market in APAC regions.
- Navigating the complexity in cell and gene therapy studies, leveraging resources on hospital infrastructure, clinicians, as well as chain logistics to ease the burden of investigators and sites.
- Exploring Fortrea’s dedicated infrastructure and expertise in the CGT arena.
Ablauf
15:00-15:15 | Landscape & Regulatory
Global CGT landscape and navigating the Regulatory Landscape
15:15-15:30 | Insights from sites
Addressing the Complexities of Conducting CGT clinical trials
15:30-15:45 | Commercialization
Advancing cutting-edge therapies from bench-to-bedside
15:45-16:00 | Operation Excellence
From Benchtop to Patient -Manufacturing Considerations for Clinical Development of Advanced Therapeutics
16:00-16:30 | Panel Discussion