
For companies currently positioning themselves in the cell and gene therapy (CGT) sector, strengthening quality management across the entire product lifecycle, exploring investment and financing opportunities, enhancing innovation capabilities, implementing efficient international expansion strategies, and maintaining operational viability have become core strategic issues that innovative pharmaceutical enterprises must urgently address amid the ongoing capital winter. Meanwhile, in the field of cell and gene therapy, technological innovation should not only focus on the advancement of the technology itself but also prioritize its real-world clinical effectiveness and patient experience.
With the rapid advancement of cell therapy technologies, the traditional centralized manufacturing model can no longer fully meet the demands of personalized treatment. There remains substantial market demand for more precise, efficient, and safer therapeutic approaches. Key challenges urgently requiring exploration in the CGT industry include overcoming traditional spatial and temporal constraints, shortening patient treatment cycles, seizing critical therapeutic windows, and alleviating the financial burden of treatment on patients.
At the same time, we also observe that Point-of-Care Manufacturing (POCM), as a disruptive innovation model, is leveragingRevolutionizing Efficiency, Practicing Inclusive Healthcare, and Safeguarding Quality Throughout the Care Continuumand other advantages are reshaping the industry landscape.
Against this backdrop, to facilitate the synergistic development of China’s and the global cell and gene therapy ecosystems, Miltenyi Biotec, in partnership with the Chinese Society for Gene and Cell Therapy (CSGCT), will host an event on March 28, 2025“International Symposium Series on Regulatory and Technical Accessibility of Point-of-Care Manufacturing (POCM) for Cell and Gene Therapies”
Conference Highlights
Breaking Through the Regulatory Fog
In-Depth Analysis of Major Global Regulatory Frameworks, Including China’s NMPA, the US FDA, and the EU EMA: A Practical Guide for Cross-Border Regulatory Submissions。
Technical Standardization Breakthrough
Focusing on the Seamless Integration of GMP Manufacturing and Clinical Applications: Sharing the Latest R&D Achievements in Automated Preparation Platforms.
Breaking Through the Commercialization Path
Dissecting the translational barriers from lab to market, unlocking the value depression in the POCM sector as seen by investment institutions.
Meeting Overview
Hosted by:Miltenyi Biotec Co., Ltd., CSGCT
Co-organizers:Beijing Haixinyu Urban Renewal Group Co., Ltd., Beijing Haixing Technology Industry Service Co., Ltd.
Supporting Organizations:Beijing Vital River Laboratory Animal Technology Co., Ltd., Shanghai Hougao Scientific Instrument Co., Ltd., Tianjin Tianda Tianfa Technology Co., Ltd.
Organizer:Eggshell Technology (VCBeat)
Meeting Time:March 28, 2025
Venue:C Zone, Haixing Pharmaceutical and Health Innovation Park, Haidian District, Beijing
Core Issues
• Global Regulatory Framework and Mutual Recognition Mechanisms for Cell Therapy POCM
• Patient-Centered Treatment Model: Clinical Application of Point-of-Care Manufacturing (POCM)
• Deep Integration of GMP Manufacturing and Clinical Applications: Core Technologies and Risk Management Strategies for POCM
• Scientific Regulation Empowering New Quality Productive Forces: Global Practices and Innovations in the Clinical Translation of POCM Cell Therapy
Meeting Agenda

Note:The final agenda will be determined on-site.
Conference Registration

This event offers free registration (subject to review).
Exquisite lunch and tea breaks will be provided for attendees during the event.
Welcome to register and join us for collaborative discussions.
Conference Contact Information
For matters regarding conference attendance, please contact the conference assistant, Danni:

Phone: 18800157211 (also WeChat)

