Founder and CEO
Dr. Li Chen, Founder, Executive Director, Chief Executive Officer, and Chief Scientific Officer. leads Hua Medicine a clinical stage biotech company whose mission is to bring personalized diabetes medicines to patients in China and worldwide. He is a pioneer in collaborative innovation in China and advanced Hua Medicine with an operation principle of high standards, high quality and create high value. Hua Medicine leverages global resources to develop GKA and completed 6 clinical studies in China and USA, in which the HMS5552, a novel GK PAM demonstrated desirable safety and efficacy profiles together with an improvement of beta cell function in Chinese T2DM patients. Under his leadership, Hua Medicine completed successfully a POC study and initiated China NDA enabling process. During this period, Hua Medicine raised 200M USD and established the leading position of Hua Medicine in China biotech industry.
Li received his PhD at Iowa State University and joined Roche R&D center in USA in 1992. With 18 years at Roche, Li advanced his career from a medicinal chemist to the head of High Throughput Technology, and later CSO of Roche China R&D Center with a membership at Roche Research Leadership Team. He is an inventor of 35 granted patents and an author with over 60 publications.
EVP & Chief Financial Officer
SVP, Regulatory, Medical Safety and Manufacture
Dr. Daniel Du has worked in pharmaceutical industry for more than 20 years with broad experience in drug discovery, clinical development and regulatory submission. He was instrumental in discovery of multiple clinical candidates and played significant roles in multiple IND and NDA submissions when he was working in two of the fortune 500 pharmaceutical companies. He is also a skilled clinician and medical monitor for clinical studies, experienced in safety management, and authored the clinical sections for multiple NDA filings. He is the inventor of over 15 patents and authored over 20 manuscripts. Dr. Daniel Du received Medical degree from Beijing Medical University and PhD of Pharmacology and Toxicology from Albany Medical College, NY. He received US Education Certificates for Foreign Medical Graduates (ECFMG).
SVP, Clinical R&D
Dr. Yi Zhang heads the clinical research & development team at Hua Medicine, and currently as the senior vice president since April 2018. Prior to joining Hua, Dr. Zhang was the Associate Medical Director of Clinical Science at Roche Product Development group, Asia Pacific region. She served as a clinical scientist for innovative drug development in the areas of cardiovascular, metabolic and renal diseases. Prior to Roche, Dr. Zhang was a Physician and an Associate Professor at Shanghai Ruijin Hospital, Shanghai Jiaotong University School of Medicine with more than 10 years' clinical experience. Dr. Zhang was also a team leader of the molecular genetics research group at the Shanghai Institute of Hypertension and a principle investigator for several projects supported by the National Natural Science Foundation of China and the Shanghai Municipal Natural Science Foundation. Dr. Zhang obtained her Doctor of Medicine and PhD degrees from Shanghai Jiaotong University School of Medicine(specialization in cardiology) She received training in molecular genetics, bioinformatics and epidemiology at the Chinese National Human Genome Center and at the Framingham Heart Study as a NIH/NHLBI visiting researcher. Dr. Zhang has received Shanghai Subject Chief Scientist and 60 publications in journals such as Nat Genet, Circ Cardiovasc Genet, Hum Mol Genet, 4 book chapters, and has 3 China patents.
Dr. Yong-Guo Li (Fred) serves as VP Pharmaceutical R&D at Hua Medicine (Shanghai) Limited and currently as the senior vice president since April 2018, an innovative biotech company focused on developing novel therapeutics. His major responsibilities include overseeing Chemistry, Manufacture & Control (CMC) and Drug Supply, GxP compliance, and supervising Corporate Project Management. Prior to joining Hua Medicine, Dr. Li worked at Roche’s R&D Center (China) for nearly 8 years as Head of Analytics and Deputy Head of the CMC Department. He also served as a member of the Senior Management Team, Research Project Management Team, Metabolic Project Leadership Team, and was an acting Officer of Environmental Safety and Health (EHS). Before Roche, Dr. Li worked at the global healthcare company Pharmanex as the Head of Analytics and Quality Assurance for 8 years. He was also a faculty member of China Pharmaceutical University for 5 years. He has published over 20 scientific articles in peer-reviewed journals and is an author of 4 book chapters. Fred is currently an Adjunct Professor at Shanghai University of Chinese Medicine.
VP, Quality Assurance
A seasoned leader in quality control and assurance with over 20 years experiences in the Pharma industry across sites and countries at AstraZeneca, Xian Janssen and Boehringer-Ingelheim (Germany & China). In his extensive knowledge and experience with proven track records for hosting various regulatory GMP, GSP inspection successfully include EU, TGA and CFDA authorities. Also Mr. Fu have rich hands-on experience for leading company Quality Culture change, continuous improvement of quality management systems and building high performing quality team. He is taking overall quality management responsibilities for Hua’s QMS systems and as executive co-chairman for Quality & Safety committee. Mr. Fu is licensed pharmacist and owns master degree of business administration from Shanghai Jiaotong University.
VP, Commercial Strategy and Marketing
Senior Director, Clinical Pharmacology
Dr. Shuang Ren is responsible for Bioanalytical, Preclinical Pharmacology, and Clinical Pharmacology at Hua Medicine. Dr. Ren has over 11 years’ experience in drug research and development at various top 10 international pharmaceutical companies as clinical pharmacologist and DMPK project leader in different disease areas (metabolic diseases, respiratory disease, oncology, CNS and infectious disease). Prior to Hua Medicine, she worked at the Novartis Institutes for Biomedical Research (NIBR) Shanghai Center as Investigator in Clinical Pharmacology, and Roche R&D Center (China) as Senior Scientist in DMPK. Dr. Ren received her PhD in molecular biology and biochemistry from Tong Ji University.
Senior Director, Preclinical Drug Safety
Dr. Haoliang Song is Director, Drug Safety Assessment at Hua Medicine. Now he is managing all the drug safety-related studies, cooperating with the partners from US, China and other countries. As a member of Hua Medicine QQLT, Dr. Song also attends the Quality control strategic development of Hua Medicine projects. Dr. Song has more than 16 years experience in hospital and biotechnology company. Before joining the company, Dr. Song worked at Medicilon as Director of Operations and Study Director to lead teams in the development of GLP and non-GLP preclinical studies. He received USFDA GLP regulation and study trainings including study design and study operations & management at US MPI RESEARCH. Prior to that, Dr. Song spent several years at Hong Kong Polytechnic University as Research associate and its institute of Modern Chinese Medicine as Head of Pharmacology department, leading teams in the development of pharmacology and toxicology techniques platform, where he completed the studies for the doctoral thesis. Dr. Song also had five years working experience in hospital, where he had more close attention on how to meet the patients’ needs. Dr. Song is the author of more than 10 publications and one of the inventors of 4 patents.
Senior Director, Industrial Policy & Regulation
Michelle is a seasoned leader in China pharmaceutical policy and regulation over 20 years in China with rich experience in market access and government policies. Prior to joining Hua Medicine, she has worked with Boehringer-Ingelheim, Abbott and J&J China operation and established her leadership in the drug price negotiation, market entry and establishment of joined ventures. She was in charge of market access affairs and responsible for developing government affairs strategies to achieve company’s business goal. Michelle has also managed government relation operation, which focused on reimbursement and pricing. She cooperated with government agencies/organizations and Industry Associations for monitoring central and provincial government policy changes.
Senior Director, Regulatory Affairs
Gary Yu，Master of pharmaceutics, senior engineer. Now he serves as Director of Regulatory Affairs in Division of Clinical Research and Development. Prior to join Hua, Gary was in charge of two developing projects of innovative T2DM drug candidates and managed a series of tasks that preclinical evaluation, clinical development and regulatory affairs are included. One of these projects was supported by National Key Technologies R&D Program and has been accomplished in 2013. Gary has more than 10 years’ experience of Medical R&D project management and Pharmaceutical license progress. Gary has also participated as inventor in writing and registration of several domestic and PCT patents.
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