
Amid the grand vision of propelling the rise of China’s cell and gene therapy (CGT) industry, Beijing has rightfully emerged as the cradle of CGT innovation and a highland for industrial development in China, leveraging its profound foundations in life sciences, top-tier clinical and research resources, vibrant innovative capital, and a robust industrial ecosystem. With foresight and unwavering determination, the Beijing Municipal Government has prioritized CGT as a key frontier in life sciences and biotechnology. By implementing a series of policy innovations, guiding patient capital, developing specialized industrial parks, and attracting top-tier talent, Beijing has established a comprehensive support system covering the entire value chain—from basic research and technology transfer to clinical trials, pilot-scale manufacturing, and commercialization. Beijing is striving to build a globally influential CGT innovation hub, providing the most fertile ground for the growth of domestic innovators while opening up the smoothest channels for advanced international technologies and capital to enter the Chinese market.
At this critical juncture, where the spirit of the times resonates in sync with national and local strategies,2025 2nd China Cell and Gene Therapy (CSGCT) Conferenceemerged as the times required,scheduled to be held inSeptember 12–13, 2025InZhongguancun National Independent Innovation Demonstration Zone Exhibition and Trading CenterGrand Opening。This conference will be themed “Rooted in Regulation, Harnessing Wisdom, Connecting Globally, Co-Creating the FutureGuided by this core philosophy, the conference closely aligns with the latest developments and scientific guidance in government regulatory policies. It deeply integrates top-tier global regulatory expertise, cutting-edge clinical research resources, substantial industrial capital, and dynamic corporate capabilities. Dedicated to building an authoritative, open, and efficient global dialogue platform, the conference enables key industry stakeholders—including policymakers, scientists, clinicians, entrepreneurs, and investors—to engage in in-depth exchanges of ideas, spark intellectual innovation, and explore collaborative opportunities. With a global perspective, we will thoroughly examine the opportunities and challenges in shaping the CGT industry ecosystem, focusing on core issues such as advances in regulatory science, breakthroughs in technological innovation, pathways for clinical translation, bottlenecks in industrialization, and strategies for global cooperation.

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Four Major Resource Advantages Working in Concert
Striking the Strongest Note in International Cooperation
This conference focuses on the latest developments and scientific guidance in government regulatory policies, conducting in-depth discussions centered on core topics such as advances in regulatory science. Numerous government and regulatory officials have gathered together, includingNational Health Commission, National Medical Products Administration, Beijing Municipal Science & Technology Commission, Haidian District People's Government of Beijingsenior officials, who will deliver authoritative insights on policy interpretation and regulatory review and approval to support industrial development, analyzingPolicy Orientation and Regulatory Guidelines, providing direction for industry development, and offering in-depth discussions on the application and interpretation of policies regarding advanced therapy medicinal products (ATMPs) and new clinical technologies, as well as the latest requirements for quality control and testing of cell and gene therapy (CGT) products across various countries, thereby delivering comprehensive and practical regulatory knowledge to practitioners.
Dr. Wu Zhenhua, the founder of CSGCT and an early participant in ASGCT, has laid a solid foundation for international cooperation for the conference. In addition, the 2025 CSGCT Conference has invited many key international guests in the field of cell and gene therapy (continuously updated), such as:
Professor Mark Kay,Professor of Human Gene Therapy and Genetics at Stanford University; Director of the Division of Human Gene Therapy at Stanford University; Co-founder of the American Society of Gene & Cell Therapy (ASGCT); Former President of ASGCT; Co-organizer of the American Society for Microbiology’s Conference on Viral Vectors; Member of the Executive Committee of the Stanford University Academic Senate. As a founding member and former president of ASGCT, he is recognized as a world-leading expert in gene therapy.
Dr. Jude Samulski,A pioneer in adeno-associated virus (AAV) research, he has dedicated over 40 years to the AAV field and was the first scientist to clone the AAV genome, a discovery that enabled researchers to begin engineering AAV into gene delivery vectors. He co-founded Asklepios BioPharmaceutical (AskBio), a company committed to developing novel AAV vectors as tools for delivering gene therapies. AskBio’s technology has been adopted by multiple companies, including Bayer, Pfizer, Takeda, and Novartis. Last October, Bayer acquired AskBio for approximately $4 billion.
Ms. Sheila Mikhail,She has served as a Director of Verve Therapeutics since April 2021. The company specializes in in vivo gene editing therapies and is dedicated to developing innovative treatments for the prevention of cardiovascular diseases using base editing technology. In 2001, she co-founded AskBio, an AAV gene therapy company, and served as its CEO from April 2017 until its acquisition by Bayer in 2020. She served as CEO of Bamboo Therapeutics, a gene therapy company, from December 2014 until its acquisition by Pfizer in November 2016. From 2010 to 2014, she was a member of the management team at Chatham Therapeutics, which was acquired by Baxter. With over 15 years of legal experience, she founded Life Sciences Law PLLC and served numerous prominent clients. She holds a Bachelor of Science degree from the University of Illinois at Urbana-Champaign, a Juris Doctor from Northwestern University, and an MBA from the University of Chicago Booth School of Business.。
In addition, key opinion leaders such as Haifeng Chen (Vice President and Chief Scientific Officer at Virovek), Zhongyu Zhu (Chief Scientific Officer at Caring Cross), and Loh Hui Pin (Managing Director at AbGenTil) have also confirmed their attendance at the conference.
The conference fully demonstrated the abundant resources of cutting-edge translational research in the field of cell and gene therapy. On one hand, top-tier domestic scientific research forces have gathered here, especiallyExperts and scholars from numerous universities and research institutes in Beijing, as well as Grade IIIA hospitals, clinicians, etc., share inBasic Research, Clinical Trials, and Translational Applications in Cell and Gene Therapylatest achievements and practical experience in areas such as gene therapy, stem cell therapy, immune cell therapy, and nucleic acid drugs. On the other hand, the conference also attracted numerous corporate guests, representing the key innovators in the cell and gene therapy industry, who possess extensive experience and resources in translating scientific research into applications. Through close interaction and collaboration between research institutions and enterprises, the conference established an efficient platform for exchanging frontier translational research resources, acceleratingTranslating Scientific Achievements from the Laboratory to Clinical Applications and the Market, driving the rapid development of the cell and gene therapy industry, and providing more effective treatment options for major diseases such as cancer and genetic disorders.

Comprehensive Coverage of Cutting-Edge Topics
Addressing Industry Pain Points and Bottlenecks
The conference closely addressed the industry’s hotspots, pain points, and bottlenecks, featuring 1 main forum + 8 high-end sub-forums, coveringGlobalization of China’s Cell and Gene Therapy Industry; Latest Advances and Applications in Global Gene Therapy, Immune Cell Therapy, Stem Cell Therapy, and Nucleic Acid Drugs; Recent Progress and Applications in CMC and Testing; Latest Clinical Exploration Advances in the Global CGT Field; AI-Driven Drug R&D; Overseas Financing Matchmaking; Interpretation of the Latest Policiesand other key issues, achieving in-depth coverage of the entire cell and gene therapy industry chain.
In the field of gene therapy, an in-depth discussion will be conductedGene Editing, Vector Optimization, and Rare Disease Therapybreakthrough achievements in the field, pointing the way for the future development of gene therapy, and will also explore gene therapy inOphthalmology、OtologyandCNSandRare Diseasestherapeutic prospects in disease areas such as... The cell therapy segment focuses onAllogeneicCAR-T,invivo CAR-T,iPSCTechnologythe application prospects of cutting-edge therapies in disease areas such as solid tumors, non-solid tumors, immune diseases, and neurodegenerative diseases, sharing the latestInnovative Design、Clinical Research Data andAdvances in Cancer Treatment. As an emerging hotspot in recent years, nucleic acid therapeutics will be featured at the conferenceFocusTherapeutic Cancer VaccinesofDevelopment and Combination Therapy,andNovel Delivery Vectors for Nucleic Acid TherapeuticsDevelopment and Indication Expansion, analyze the key scientific issues in the R&D process of nucleic acid drugs and the challenges faced in industrialization, to facilitate the translation of this field from laboratory to clinical practice and market.
Due to their inherent characteristics and complexity, the manufacturing processes of cell and gene therapy (CGT) products are more complex than those of small-molecule chemical drugs or other biologics. Challenges such as testing of final CGT products, product release testing, and specification setting have long been persistent difficulties in the early-stage development process for companies. In light of this, the conference has specially organized a forum on the latest advances and applications in CMC and testing within the global CGT field, which will focus onFrontier Innovations and Development Trends in Manufacturing Processes and Quality Characterization of CGT Products、How to Build a CompliantCommercialized Production System for CGT Products with Market-Oriented Characteristics (Process Validation, MAH Category B License, Production Line Design, etc.)Frontier Innovations and Development Trends in CGT Product Manufacturing Processes and Quality CharacterizationWaitIn-depth analysis to help enterprises tackle critical CMC challenges in the product development lifecycle and overcome quality compliance barriers in CGT product development.
Looking at the landscape in China and globally, an increasing number of companies are beginning to lay out their CGT (Cell and Gene Therapy) pipelines. How to substantially address the issue of commercial accessibility of products has become the most clear-cut challenge facing the industry today. In light of this, the 2025 CSGCT Conference will bring “How to PromoteAchieving a Sustainable Commercialization Pathway in the CGT Sector" cross-domain dialogue,AnalysisProductBreakthrough Points for Commercial Value,ExploreProductImplementationBusinessTransformationYesEfficacyandHigh EfficiencyofPathways and Patterns。
Meanwhile, the conference also focuses on the enabling role of AI technology in cell and gene therapy, analyzing how AITarget Discovery, Drug Design、Vector Constructionand production automationapplication potential in these areas, offering new perspectives for the industry’s digital transformation. For enterprises, overseas financing serves as a crucial support for achieving technological breakthroughs and market expansion. To this end, the conference has specially organized the China Biotech Overseas Financing Matchmaking Conference and CGT Project Roadshows to analyzeCore Logic of CGT Product Pipeline Layout and Value Investment, to establish a precise matchmaking platform for domestic enterprises and overseas investment institutions, helping companies broaden their financing channels and accelerate their international expansion.
The closed-door policy interpretation session brings together experts from regulatory agencies,In-Depth Analysis of the Latest Product Registration Trends and Regulatory Dynamics in Cell and Gene Therapy in China and AbroadPolicy and Regulatory Requirements, helping enterprises achieve compliant development and mitigate risks, while driving innovation and sustainable growth in the industry under policy support.

Whole-Chain Resonance, Venture Capital Co-Field

Distribution Map of Core Attendees
In-Depth Exploration Tour of China's CGT Industry
Clinical Practice, Policy Interpretation, and Global Collaboration

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2025Year9Month12-13Day
2025 2nd China Society for Gene and Cell Therapy (CSGCT) Conference
Golden Autumn in September, Gather in Haidian, Beijing!
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