Biography
Anand has over 14 years of research experience in the pharmaceutical industry including generics and New Chemical Entities (NCE) development, scale up, technology transfer, registration, where he was involved in the overall end to end project management. He is currently working as a Director and Head of Formulation Development at BioDuro and supporting Yangtze River Pharmaceutical Group for formulation related technologies. Prior to joining BioDuro Anand worked over 7 years as a Director of Pharmaceutical Development Services at WuXi AppTec, Shanghai. In this role he was involved in building the formulation development team and infrastructure to support various dosage form development and pilot scale manufacturing. He also worked with over 35 global clients and over 120 projects to support various stages of clinical development. He was involved as a key SME for successful MPA (EU), US-FDA and C-FDA site inspections for GMP. He was also involved in successfully implementing several key technology platforms including microdoser, hot melt extrusion (HME), bilayer tableting, spray drying etc. He has received “Best team management†award in the year 2013. He is a recipient of several prestigious awards.
Research Interest
Pharmaceutical development focused on poorly soluble compounds as well as successful pharmaceutical project management and contributes in overall CMC development.
Biography
Likun got his Bachelor’s degree in Biomedical Devices and PhD in Industry Pharmacy with focus on PAT, imaging, pelletization and coating process. Likun Joined Johnson & Johnson Pharmaceutical Research & Development (Belgium Site) in 2011 and act as scientist to develop and manage automated screening platforms for early development. In 2014, Likun became senior scientist and preformation group leader for automated screening and early development. In 2015, Likun joined Jiangsu Hengrui Medical co. as NanJing R&D site director and returned to China. Hengrui Nanjing R&D site is responsible for preformuation & early development for NMEs, formulation innovation for generics as well as external collaborations and innovation with Universities and research Institutes.
Research Interest
Preformulation & early development, Polymorphism & Salt, Enabling formulation & Processing of small molecules (Amorphous Solid Dispersion, Nano-suspensions, Lipid system), High throughput screening, Biopharmaceutics & PBPK Modeling, Material Characterizaiton & Physical Stability, Controlled Release formulation development, Chemometrics & PAT, Fundamental Understanding of physical stability
Biography
Dr. Jinming Gu obtained his Ph.D. degree in Molecular Biology from Vanderbilt University. He then joined Dana-Farber Cancer Institute/Harvard Medical School for a postdoctoral training in oncology. Dr. Gu started his industry career at Merrimack Pharmaceutical, Inc., where he worked on MM111, a bispecific antibody currently in Phase 2 clinical trial. He then joined Abbott Laboratories. Since joining Abbott/Abbvie, he has been leading/working on multiple mAb, ADC, and bispecific antibody programs, including ABT-806, ABT-414, and ABT-165 etc. Dr. Gu is currently the Executive Director of Biologics Discovery at Shanghai Hengrui Pharmaceutical Co., Ltd., a leading innovative pharmaceutical company in China.
Research Interest
Research Interest: Pharmaceutical R&D; Biologics Drug Discovery and Development, Cancer Immunotherapy, Biosimilar, Biobetter.