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    With field research of markets and industries which is analyzed from a global strategic perspective by our professional teams, as well as hot topics which interest leadership and management, Shine Consultant provides you with one-stop platform of dialogue, practice -sharing and social network!
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    Committed to provide keynote speakers, executive learning masterclasses and boardroom advisory for global enterprises and institutions, each service provides a deeper and more interactive experience, especially for small, selected audiences and key individuals. We have the resources of the most influential business leaders and experts, who are the most outstanding representatives in their fields. Our team consists of experienced speech and event managers, and we focus on building long-term and in-depth partnerships.
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    As world-class insight network, we connects clients-decision makers with vetted subject matter experts-advisors. Our clients leverage the insights and perspectives shared by our advisors to stay informed and make better business decisions.We have over 600,000 Shine Advisors in 20 industries, which continues to grow every day.
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    Committed to be the world's most professional provider of industrial Summit & Event. We provide one-stop professional services, including investigating and planning, on-demand inviting, marketing and promoting, operating, project management, live& digital conference, each service is performed by an experienced professional team matched with long-term industrial resources. We focus on establishing long-term and in-depth partnerships.
Guest Information
发布时间: 2018 - 11 - 09
点击次数: 0
Positions:
Company: BlueRock Venture Partners
个人简介:
John Niu is a co-founder of BlueRock Venture Partners and focuses on advances in biotech and drug innovation. He has been actively identifying and evaluating new investments and has played key roles in launching, building and developing strategy of new companies. John is also the president and chief executive officer of McCull Pharmaceuticals and founding director at a number of startup biotech companies. Prior to the founding of BlueRock Venture Partners, John served as a Managing Director of GM Capital and as director and interim CEO of Chinda Biological. Prior to the founding of McCull Pharmaceuticals, John worked with Sanofi-Aventis and Merck and held a variety of roles of increasing responsibility in pharmaceutical research and development. John also played a key role in leading SUBIA (Sino-US Biomedical Investment Association) for promoting innovation and capital investment cross the border of US and China. John received his Ph.D in Chemistry and Toxicology from Iowa State University in US and a B.S. in Organic Chemistry from Zhengzhou University in China.John has over 20 years of experience in the pharmaceutical-biotechnology industry and assumed various active leadership roles as research scientist, executive, entrepreneur, and venture capitalist. He concentrates primarily on venture-funded biotech asset and early discovery platform with investment approaches of “Asset-Centic” and “Build-to-Exit” philosophy.As a serial entrepreneur, John founded PharmaSolution LLC in New Jersey in 2005, a Delaware incorporation - McCullough Pharmaceuticals Inc in 2008, McCull Nantong in 2011, and Rudong KeBio in 2015. He served as founding Director and CEO and played key role in the early sourcing, financing, launching and development of the start-up companies. In these roles, he was instrumental in formulating the initial business plan and assembling the founding team, and directed drug innovation and product development of recombinant proteins and antibodies anticancer-drugs and new anti-coagulation biochemical drugs. Through these endeavors, John gained extensive strategic and operational experience in startup biotech companies.Prior to the founding of McCull Pharmaceuticals, John worked with Sanofi-Aventis and Merck and held a variety of roles of increasing responsibility in pharmaceutical research as a research chemist, senior scientist, study director, and the Chair of the global CMC team. Through his career, he participated in a large number of R & D projects from small molecule to biochemical drug development. He gained broad expertise across all phases of drug discovery, early development and process sciences, As chairman of the global CMC team, he was responsible for coordinating activities for global strategic planning, technical development, outsourcing and cooperation with cross-department members from Chemical Development, Pilot Plant production, Toxicology,DMPK, Drug formulation, Analytical Science, Clinical Supply Chain, Regulatory Affairs, and GMP Compliance. While working at Sanofi-Aventis, he pursued his QA/RA MS program studies from Temple University School of Pharmacy and obtained the RA/QA certificate in May 2007. John started his pharma career with Sanofi in 1995, joined Aventis in 2008, and then entered Sanofi-Aventis at Bridgewater NJ in 2001 due to company merge.John received his Ph.D in Chemistry and Toxicology from Iowa State University, and a B.S. in Chemistry from Zhengzhou University. He had been a research staff at Ames Laboratory US-DOE since 1989 and was formerly a lecturer in Organic Chemistry at Zhengzhou University. John is an adjunct professor of Nantong University.
发布时间: 2018 - 11 - 09
点击次数: 0
Positions:
Company: Beijing InnoCare Pharma Tech. Ltd.
个人简介:
Dr. Jasmine (Jisong) Cui is the co-founder, President & CEO of Beijing InnoCare Pharma Tech. Ltd. Dr. Cui is the expert of National Thousands Talents Plan and Beijing Specially Recruited Experts. InnoCare is a biopharmaceutical company rooted in China with the global vision to discover and develop novel treatment for cancer and autoimmune diseases.Prior to founding InnoCare, Dr. Cui was the General Manager of BioDuro (2011-2015). Her area of responsibility included BioDuro’s overall scientific and operational management, as well as business & resource management. Before BioDuro, Dr. Cui worked at Merck Research Laboratories for 14 years serving as Director of Cardiovascular Diseases where she provided project leadership for delivering 10 drug candidates. She also served as the Chair of Early Development Team for development of drug candidate from preclinical to clinical phase 2a for POC in humans. Additionally she headed the hypertension exploratory biomarker for identifying and developing preclinical and translatable biomarkers in cardiovascular diseases.Dr. Cui received her Ph.D. in biology from Purdue University and completed her postdoctoral fellowship at Howard Hughes Medical Institute affiliated with the University of Michigan. Dr. Cui was the 17th SAPA President with the honor to be the first female President in the history of SAPA. Currently, Dr. Cui is the president of SAPA China.-founder, President & CEO of Beijing InnoCare Pharma Tech. Ltd. Dr. Cui is the expert of National Thousands Talents Plan and Beijing Specially Recruited Experts. InnoCare is a biopharmaceutical company rooted in China with the global vision to discover and develop novel treatment for cancer and autoimmune diseases. Prior to founding InnoCare, Dr. Cui was the General Manager of BioDuro (2011-2015). Her area of responsibility included BioDuro’s overall scientific and operational management, as well as business & resource management. Before BioDuro, Dr. Cui worked at Merck Research Laboratories for 14 years serving as Director of Cardiovascular Diseases where she provided project leadership for delivering 10 drug candidates. She also served as the Chair of Early Development Team for development of drug candidate from preclinical to clinical phase 2a for POC in humans. Additionally she headed the hypertension exploratory biomarker for identifying and developing preclinical and translatable biomarkers in cardiovascular diseases.Dr. Cui received her Ph.D. in biology from Purdue University and completed her postdoctoral fellowship at Howard Hughes Medical Institute affiliated with the University of Michigan. Dr. Cui was the 17th SAPA President with the honor to be the first female President in the history of SAPA. Currently, Dr. Cui is the president of SAPA China.
发布时间: 2018 - 11 - 09
点击次数: 0
Positions:
Company: Elpiscience Biopharma
个人简介:
Dr. Hongtao Lu is currently co-founder and Chief Scientific Officer (CSO) of Elpiscience Biopharma, a biotech company focusing on immuno-oncology. Trained as an immunologist and a 20-year industry veteran, he has worked on several therapeutic areas (autoimmune diseases, oncology and neuroscience) using both small-molecule and biological approaches. Before Elpiscience, he had spent four years with Zai Lab, a NASDAQ-listed company, as co-founder and CSO and helped to build a robust pipeline focusing on oncology and autoimmune diseases. Prior to Zai Lab, he was with GlaxoSmithKline as the founding head and senior director of Neuroimmunology Discovery Performance Unit (NI-DPU), where he led about 70 biologists and chemists focusing on drug discovery in multiple sclerosis and other neurodegenerative diseases including Parkinson's disease and had successfully built the team and the pipeline from scratch in 5 years with four clinical assets and four pre-clinical programs.Dr. Lu spent his early career with Berlex Biosciences and Bayer Schering Pharma, where he conducted target identification and validation in autoimmune inflammatory diseases and oncology. Dr. Lu holds a Ph.D. in Regulatory Biology and conducted his graduate research at the Cleveland Clinic Foundation, focusing on MHC class II gene regulation followed by post-doctoral fellowship at Yale University School of Medicine under the guidance of Dr. Richard Flavell, working on T cell differentiation and signal transduction pathway. He got his Bachelor degree at the Biology Department of Xiamen University in 1987.
发布时间: 2018 - 11 - 09
点击次数: 0
Positions: Chairman & CEO
Company: BioNova Pharmaceuticals Ltd
个人简介:
Ye Hua, MD, MPH is the founder and CEO of BioNova Pharmaceuticals, a start-up biotech drug company that is focused on drug development to fill the gap of unmet medical needs in oncology and other diseases. Prior to building up BioNova, he was Senior VP, Head of Clinical Development and Regulatory Affairs at Hutchison MediPharm, a leading R&D company in oncology and autoimmune diseases. Managing the clinical and regulatory organization, Dr. Hua is responsible for advancing clinical development pipeline and registering new drugs in China and ex-China. Under his leadership, the clinical development programs have grown from 5 small molecules in 7 Phase 1 oncology clinical trials to 8 small molecules in over 30 Phase 1-3 clinical trials in oncology and immunology in China, Australia, and USA. Most recently, Dr. Hua led fruquintinib NDA submission in mCRC indication via MAH policy and received NMPA approval. Native from Shanghai, Dr. Hua graduated from Fudan University Shanghai Medical College in 1992. He worked as a cancer epidemiologist at Shanghai Cancer Institute between 1992 and 1996, and then went to McGill University in Montreal Canada to pursue a Master Degree in cancer epidemiology. Dr. Hua is a senior clinical research physician who has over seventeen years’ global clinical development and new drug registration experience in the pharmaceutical industry. He started his career in the pharmaceutical industry as a biostatistician at Pharmacia & Upjohn in 1999, and worked through the rank in biostatistics. His most significant achievement being the statistical team leader for the pivotal Phase 3 RA registration trial of Humira that won regulatory approval in the US and EU. Often contributed to clinical programs beyond his role in statistics, Dr. Hua was well recognized and greatly appreciated by cross-functional development teams. In 2004, one year after joining Novartis, Dr. Hua successfully switched career track back to clinical. Being a medical monitor, he led a number of global Phase II/III registration trials in osteoarthritis, osteoporosis, infectious diseases, oncology and hematology disease areas. As clinical project leader, Dr. Hua contributed to the regulatory approval and life-cycle management for Reclast/Aclasta, Prexige, Zometa, Femara, Proleukin and Cardioxane in the US and EU. His last job in the US was Senior Director, Global Clinical Development, Celgene Corporation where he led several global clinical teams for Revlimid and Pomalyst NDA/sNDA in multiple myeloma indication, and eventually obtained regulatory approval in the US and EU. In addition, he led clinical subteam executed registration trials for Revlimid and Pomalyst in China, and successfully obtained Revlimid regulatory approval in multiple myeloma indication.