
Innovative Formulation Developer

mRNA technology has garnered significant industry attention due to its outstanding application outcomes, and nucleic acid therapeutics have evolved from a frontier research direction into a key global track for new drug development. As the industry enters a phase of in-depth development, numerous challenges have emerged:
How can mRNA therapeutics expand their application scenarios and establish a presence in therapeutic areas such as oncology and autoimmune diseases? How can small nucleic acid therapies break through the market limitations of rare diseases and enter the vast blue ocean markets of oncology, central nervous system disorders, and chronic diseases? How can we achieve true large-scale breakthroughs in the critical bottlenecks of delivery systems and manufacturing processes?
September 4-5, 2026,[CBI2026 Biopharmaceutical Innovation Expo – Nucleic Acid Drug Innovation Development Conference]The event will be held at the Suzhou International Expo Center. Co-hosted by Weichun Technology and Pharmapharm Circle, this conference focuses on two core themes: mRNA drugs and vaccines, and small nucleic acid drug development. It brings together seasoned industry professionals to break down barriers across the entire chain of technological R&D, clinical development, and process manufacturing, thereby mapping out the path for nucleic acid therapeutics from technical validation to large-scale commercialization. Registration is now open—join us for on-site exchanges!

Forum Name:CBI 2026 Nucleic Acid Drug Innovation and Development Conference
Forum Time:September 4-5, 2026
Forum Venue:Hall B, Booth B104, Suzhou International Expo Center
Co-organizers:MicroPure Technology, PharmNet Circle


*Sorted alphabetically by first letter of name (A-Z); no special significance intended.

Professor Song Xiangrong, Ph.D. in Pharmaceutics, Postdoctoral Fellow in Biology, Visiting Scholar in Nanomedicine and Immunology at Harvard Medical School, currently serves as a Principal Investigator/Doctoral Supervisor at the State Key Laboratory of Biotherapy, Sichuan University. He has been selected as a National Young Talent, serves as the Chief Scientist for the National Key R&D Program, and is the General Manager/Scientific Founder of Weijin Biotech.
With nearly 20 years of experience in the research and development of innovative drugs based on targeted delivery, I have published over 70 first-author or corresponding-author SCI papers in journals such as Nat Nanotechnol, Nat Comm, and Sci Adv. I have filed 107 invention patent applications (including 29 international patents). The nano-adjuvant (WGa01) that I spearheaded has obtained Emergency Use Authorization (EUA) for market launch in China. I have led the development of a Class 1 mRNA nano-drug, securing one approval for Phase II clinical trials and four approvals for Phase I clinical trials, with three candidates currently entering clinical trial studies. Additionally, I obtained two clinical trial approvals for small-molecule targeted drugs in China. I led the team to win the Excellence Award (the highest honor) in the 2022 National Disruptive Technology Innovation Competition organized by the Ministry of Science and Technology of China. I serve as an Editorial Board Member for Signal Transduction and Targeted Therapy, Asian Journal of Pharmaceutical Sciences, and European Journal of Pharmaceutical Sciences; a Committee Member of the Nucleic Acid Drug Branch of the Chinese Pharmaceutical Association; a Young Committee Member of the Pharmaceutics Professional Committee of the Chinese Pharmaceutical Association; a Committee Member of the Nano Biotechnology Branch of the China Medical Biotechnology Association; and the Chairman of the Western Innovation Center of the Sino-American Pharmaceutical Professionals Association (SAPA).

Ph.D. from Zhejiang University, responsible for the preclinical development of Haichang Biotech’s nucleic acid innovative drug pipeline. Published 8 SCI-indexed papers and filed over ten invention patents. The HC016 project, led in its development, has entered Phase I clinical trials, with multiple other projects in the IND-enabling stage. Research interests include the application of siRNA, ASO, and microRNA-based therapeutics in metabolic diseases, oncology, and CNS disorders. Possesses in-depth expertise in sequence design, chemical modifications, and delivery systems for oligonucleotide drugs.

Shuqing Chen, Ph.D., is a Professor and Doctoral Supervisor at the College of Pharmaceutical Sciences, Zhejiang University. He serves as a Standing Committee Member of the Pharmacogenomics Professional Committee of the Chinese Pharmacological Society and as the Honorary Chairman of the Biochemical Pharmaceuticals Professional Committee of the Zhejiang Pharmaceutical Association. He has published 240 papers in prestigious domestic and international journals, including Cell, Nature Communications, Advanced Materials, and Biomaterials, and has served as editor-in-chief or contributing editor for 16 books and textbooks. He has presided over five projects funded by the National Natural Science Foundation of China (including two Key Projects), two sub-projects under the National Major Special Project for Major New Drug Development, and one key project under the National Key R&D Program’s “Precision Medicine Research” special initiative. He has completed five major scientific research achievements, receiving the Third Prize of Zhejiang Provincial Scientific and Technological Progress Award twice, the Second Prize of Zhejiang Provincial Scientific and Technological Progress Award once, the Second Prize of Zhejiang Provincial Natural Science Award once, and the Third Prize of Zhejiang Provincial Natural Science Award once. He was selected as a Leading Talent in Scientific and Technological Innovation in Zhejiang Province. The personalized cancer vaccine he designed from scratch has received clinical trial approval from both the Center for Drug Evaluation (CDE) in China and the U.S. Food and Drug Administration (FDA), and clinical trials are currently underway.

Dr. Du Zhiqiang (Danny) serves as the Company’s Chief Operating Officer, with overall responsibility for pipeline development of innovative small nucleic acid therapeutics, optimizing and accelerating the industrialization of the pipeline, and promoting and expanding the Company’s international collaborations and comprehensive influence.
Seven-Year Integrated Bachelor’s and Master’s Program in Clinical Medicine, China Medical University
Attending Physician, Shengjing Hospital of China Medical University
Ph.D. in Biology, Texas Tech University, USA
Postdoctoral Fellow in Tumor Biology, The University of Texas MD Anderson Cancer Center
Core R&D Role at a Renowned MNC Pharmaceutical Company
Vice President of R&D at a Major Domestic Listed Pharmaceutical Company
Dr. Du Zhiqiang has nearly 20 years of experience in drug R&D and industrialization operations, having served in core R&D roles at renowned multinational pharmaceutical companies such as Novartis, Johnson & Johnson, and Amgen. In recent years, he has served as Deputy General Manager, overseeing R&D, at major domestically listed companies Shanghai Renhui Bio-Pharmaceutical Co., Ltd. and Tonghua Dongbao Pharmaceutical Co., Ltd. Dr. Du possesses extensive expertise in pharmaceutical R&D, regulatory submissions, clinical medicine, industrial development, and corporate operational management, with particularly profound understanding and accomplishments in the field of chronic diseases.
Dr. Du Zhiqiang has joined Xuanjing Biologics as Chief Operating Officer (COO). He will be primarily responsible for: the initiation of R&D projects for the company’s innovative pipeline and its forward-looking, strategic layout; leading the R&D Center in preclinical research, regulatory submissions, clinical development, and the liaison and maintenance of related resources for the pipelines under investigation; and promoting and expanding key initiatives in the company’s international operations, collaborations, and development.


Dr. Hu Rongkuan, Founder and CEO of StarryMed, is a Senior Engineer with Professorial Rank. He serves as an Industry Professor at the School of Biomedical Engineering, University of Science and Technology of China, and at the School of Pharmaceutical Sciences, Soochow University. Dr. Hu has long been engaged in the research and development of nucleic acid therapeutics and mRNA vaccines, leading the development of multiple RNA-based drugs into clinical and commercialization stages. He has filed numerous patents and published over 60 SCI-indexed papers. Dr. Hu has been honored with titles such as Jiangsu Province’s “Double Innovation Talent,” Suzhou City’s “Gusu Innovation and Entrepreneurship Leading Talent,” and Suzhou Industrial Park’s “Science and Technology Leading Talent.” He earned his Ph.D. from the University of Science and Technology of China, completed an EMBA at CEIBS (China Europe International Business School), and conducted postdoctoral research at the University of Texas Southwestern Medical Center.

Former Executive President of Fosun Pharma, Global President of R&D and Chief Medical Officer, Chair of the Scientific Committee, and Fosun Global Partner. In early 2020, he spearheaded the collaboration between Fosun Pharma and German BioNTech, participating in the development of the world’s first mRNA COVID-19 vaccine. He directly led the R&D of this vaccine, Comirnaty (Fubitai), in Greater China, as well as its market launch in Hong Kong, Macao, and Taiwan, thereby driving the development of China’s mRNA industry. He previously provided direct leadership for the global R&D and commercialization of multiple blockbuster small-molecule and biologic anticancer drugs, including Ixazomib and Isatuximab, and oversaw the R&D and market approval in China of several innovative drugs such as Izalomid and Avatrombopag. In 2013, he pioneered a clinical registration model for China-extension trials within global Phase III clinical studies, paving the way for the direct registration and market approval of innovative drugs in China using global Phase III clinical data. He has received more than 20 awards, including the Fourth Translational Medicine International Cooperation Award and the International Young Scientist Award for Gastrointestinal Cancer. He has published over 100 papers (including in The New England Journal of Medicine, The Lancet, and Nature Medicine) and authored or edited eight monographs in Chinese, English, and Japanese. He formerly served as Global Vice President of Sanofi, Director of the Shanghai Key Laboratory for Stem Cell Therapy, and Deputy Director of the Oncology Committee of the China Pharmaceutical Innovation Promotion Association.

Formerly served as a graduate supervisor at the Beijing Institute of Genomics, Chinese Academy of Sciences; Principal Investigator of the Ministry of Science and Technology’s “Innovation 2020” Vaccine Project; Chief Scientist for the National 13th Five-Year Plan Major Special Project on Infectious Diseases. Participated in the 11th Five-Year Plan Major Special Project on Drug R&D; led projects under the 12th and 13th Five-Year Plans for the “Major New Drug” Creation Initiative. Currently conducting multiple research projects funded by the Ministry of Science and Technology and local science and technology commissions. Serves as a review expert for the National Natural Science Foundation of China and provincial natural science foundations in Zhejiang, Fujian, and other provinces; serves on the editorial boards of several journals; has published more than 60 SCI-indexed papers. The Qichensheng team has over ten years of experience in investigator-initiated exploratory clinical studies in the field of cancer vaccines.

Lu Hang is the CEO of Jiayi Biotech, which focuses on the innovative development and industrialization of biopharmaceutical products based on mRNA technology and antibody platforms, and has established a development platform for preventive and therapeutic biological products.
Dr. Lu Hang has worked at EBSI and Merck in the United States for over 20 years, serving as Director or Chief Scientist. As a technical leader or core team member, he has been responsible for multiple stages of the full lifecycle development of more than ten traditional and next-generation vaccine and biological products, including CYFENDUS, which received FDA approval in 2023.
Lu Hang is an advisor to the Vaccine Basic Research Professional Committee of the China Vaccine Industry Association, former president of the Chinese Biopharmaceutical Association (CBA), and president of CBA-China.

Dr. Weiwei Tian currently serves as Vice President of R&D at Sinocan Group and General Manager of Sinocan Pharmaceuticals (Suzhou). His research primarily focuses on the creation of novel small interfering nucleic acid drugs and the development of delivery technologies. He earned his Ph.D. in Organic Chemistry from the University of Delaware in the United States and conducted pharmaceutical-related research at The Scripps Research Institute (TSRI) in the U.S. and the Agency for Science, Technology and Research (A*STAR) in Singapore.

Mr. Zhuocheng Tu has over nine years of experience in investment banking and private equity investment. He previously worked at Fengchuan Capital, where he led and participated in investments in life and health projects. Prior to joining Fengchuan Capital, Mr. Tu served in the Investment Banking Departments of China International Capital Corporation (CICC) and Haitong International, participating in various projects including initial public offerings (IPOs) and mergers and acquisitions (M&A) for multiple companies listed on the A-share, Hong Kong, and U.S. stock markets. Mr. Tu holds a Bachelor’s degree in Economics from Shanghai University of Finance and Economics.

Dr. Li Wang, who holds a Ph.D. in Immunology and graduated from the Academy of Military Medical Sciences, currently serves as Vice General Manager of Xuanzhu Biotechnology Co., Ltd. She oversees business units including small nucleic acid development, clinical development, and business development. With over 15 years of experience in new drug development and related fields, she possesses comprehensive expertise in managing the entire drug development lifecycle, from early-stage research and project initiation to commercialization. Long committed to the research and development of novel therapeutics for major diseases such as cancer and metabolic disorders, she has played a pivotal role in building the company’s innovative drug pipeline, advancing clinical development, and driving business expansion. Dr. Wang has led the R&D efforts for multiple innovative drugs at Xuanzhu Biotechnology, facilitating the market approval of three innovative drugs across multiple indications and securing overseas licensing deals. She brings extensive experience in project initiation, formulation of differentiated development strategies, execution of preclinical and clinical development, and out-licensing/collaborative partnerships.

He Wenjun, General Manager of the Chromatography Division at Weichun Biotechnology (Guangzhou) Co., Ltd., is a seasoned professional in the scientific instrumentation industry.
Holds a Master’s degree in Medicinal Chemistry from the Chinese Academy of Sciences, with nearly a decade of experience in scientific instrument market development. Has deep expertise in the chromatography industry, combining solid technical proficiency with strong business acumen.
Proficient in technology-driven sales, with the ability to accurately identify customer pain points in chromatographic analysis and provide tailored solutions. Possesses team management experience and excels at leading teams to achieve high-performance targets. Committed to advancing the market adoption of domestically produced scientific instruments and consumables through professional product expertise and efficient marketing strategies.

— Master’s degree from Peking University Health Science Center; MBA from Harvard University.
— Formerly served as Deputy Director of the Beijing Product Design Center of Taiji Group, and Secretary of the Board of Directors of the Taiji Anti-Cancer Science Foundation,
— Joined 3D Medicines in 2016, successively serving as Head of Regulatory Affairs and Deputy General Manager.
— Member of the Hong Kong Investor Relations Association; Member of the 4th Pharmaceutical Innovation Investment Professional Committee of the China Pharmaceutical Innovation and R&D Association (PhIRDA).

Dr. Xiong Changyun holds a Ph.D. from the Shanghai Institute of Biochemistry, Chinese Academy of Sciences, and completed his postdoctoral fellowship at the National Cancer Institute (NCI) of the U.S. National Institutes of Health (NIH). He has previously held positions at renowned pharmaceutical companies including BD, Novartis, Amgen, and Aim Vaccine. Currently, he is the Founder and CEO of Ningbo Junjian Biotech. With over two decades of experience in the biopharmaceutical industry, Dr. Xiong has led the research, development, and industrialization of multiple COVID-19 vaccines and antibody drugs, with a focus on self-amplifying mRNA technology. He has published more than 20 academic papers and holds over 20 invention patents, specializing in end-to-end biologic drug development, process scale-up, and commercialization.

B.S. in Pharmacy, West China University of Medical Sciences (1992); M.S. in Neuropsychopharmacology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences (1995); Ph.D. in Neuropsychopharmacology, Baylor College of Medicine, USA (2000); Postdoctoral Fellow, Department of Neurobiology, Duke University, USA (2000–2003). Currently Senior Investigator at the Center for Excellence in Brain Science and Intelligence Technology/Institute of Neuroscience, Chinese Academy of Sciences, and Shanghai Research Center for Brain Science and Brain-Inspired Intelligence; Distinguished Professor at the University of Chinese Academy of Sciences, ShanghaiTech University, and Shanghai Jiao Tong University. Standing Director of the Chinese Society for Neuroscience; Vice Chair of the Basic and Clinical Neurology Branch and the Basic and Clinical Psychiatry Branch of the Chinese Society for Neuroscience; Standing Committee Member of the Pharmacotherapy Committee of the China Anti-Epilepsy Association. Research interests include elucidating mechanisms of neurological disorders and developing innovative therapeutics, as well as establishing non-human primate models of brain diseases, objective biomarkers, and evaluation paradigms. Author of over 100 peer-reviewed publications and holder of more than 20 granted patents.

Ph.D. in Medical Genetics from Uppsala University, Sweden; Postdoctoral Fellow in Cancer Genetics and Neurogenetics at the University of California, San Francisco/Los Angeles; Former Research Fellow in the Division of Rheumatology, Department of Medicine, School of Medicine, University of California, San Diego. Upon returning to China, appointed as Qianjiang Scholar Distinguished Professor and Researcher at Shenzhen Research Institute of Sun Yat-sen University. Currently serves as Industry Professor at the Center for Cell and Gene Therapy Research, Southern University of Science and Technology. Founder of Ruimeiona (Guangzhou) Biopharmaceutical Technology Co., Ltd., with long-term engagement in the research and development of cancer genomics, cancer mRNA vaccines, and large RNA models.

Dr. Xudong Yuan is the Founder and CEO of ACON Pharma. He earned his Ph.D. in Pharmaceutics from the College of Pharmacy at the University of Georgia in the United States. After graduation, he served at Nova Southeastern University and the LIU College of Pharmacy, engaging in pharmaceutical research for many years, with a particular focus on nucleic acid drug delivery systems. Dr. Yuan subsequently transitioned from academia to the pharmaceutical industry, holding various positions as a pharmaceutical scientist at Johnson & Johnson, RB, and GlaxoSmithKline, where he participated in the research and product development of different drug dosage forms and modified-release technologies. He also served as Research Director and Vice President at pharmaceutical companies in New Jersey and Philadelphia, primarily overseeing the development of complex formulations such as liposomal, nanoparticle, nanocrystal, and microsphere-based injectables, as well as ophthalmic solutions and nasal sprays. In these roles, he was fully responsible for the R&D, manufacturing, and regulatory submission of drug products. In 2020, Dr. Yuan founded ACON Pharma, which focuses on the research and development of siRNA and mRNA nucleic acid therapeutics and complex drug delivery systems.

Topic 1: mRNA Drugs and Vaccines

- Key Considerations for Non-Clinical Studies in Vaccine and Drug Development
mRNA Vaccine Development in the Autoimmune Field
Research Progress of mRNA Vaccines in the Field of Cancer Treatment
Applications of LNPs in the Development of Novel mRNA Therapeutics
Application of mRNA Technology in Integrated Genomics
Development of Self-Replicating mRNA Vaccines
AI-Driven mRNA Vaccine Development
Strategic Analysis and Practical Considerations for Clinical Trials
Quality Research Strategy for mRNA Drugs
mRNA Drug Process Development and Manufacturing
Topic 1: Development of Small Nucleic Acid Drugs

From Technological Innovation to Clinical Research of Small Nucleic Acid Drugs
Applications of Small Nucleic Acid Drugs in Cancer Therapy
Construction of Differentiated R&D Strategies for Small Nucleic Acid Drugs
Opportunities and Challenges for Small Nucleic Acid Drugs in China
Research and Development of Small Nucleic Acid Drugs for the Central Nervous System
Breakthroughs and Frontier Advances of Small Nucleic Acid Drugs in the Treatment of Chronic Diseases
Breakthroughs in siRNA Therapy for Chronic Diseases
Development of Mass Spectrometry Analytical Methods for Small Nucleotide Drugs
Quality Control of Oligonucleotide Solid-Phase Synthesis
Challenges in Nucleic Acid Drug Quality Control and Case Studies
Research on the Delivery Stability of Oligonucleotide Drugs


With over 20 years of extensive experience in the field of chromatography, Weichun Technology has mastered leading high-pressure chromatographic packing technologies. Its product portfolio comprehensively covers the entire process from analytical to industrial-scale preparation, providing global pharmaceutical companies with analytical testing and purification solutions spanning research and development, clinical trials, and industrial manufacturing.
The company achieves full-chain independent production from microspheres to finished products, ensuring stable product quality and reliable supply. Company MicroPulite®Series Analysis Chromatography Columns and PrePulite®The performance of our preparative chromatography resin series rivals that of top international brands, with products exported to over 20 countries and regions worldwide. Leveraging an annual production capacity of 25 tons of silica-based chromatography resins, we ensure stable supply and rapid delivery. Our comprehensive product portfolio precisely meets the critical needs of the pharmaceutical industry, from R&D to large-scale production, facilitating seamless process transfer and scale-up for our customers.
Weichun Technology is committed to supporting global pharmaceutical R&D and manufacturing with cost-effective products, a reliable supply chain, and efficient services, benefiting hundreds of millions of users.


Registration:
ConferenceLimited-Time Free Access(Limited spots; first-come, first-served. This registration is a pre-registration; successful registration is confirmed upon approval of the application.) Accommodation and meals are at the participant’s own expense.

