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Next-gen Cell and Gene Therapy Discovery & Research | |
What you will learn: ★ R&D and technology progress of T cell, NK, TIL cell therapy ★ The hottest screening, preparation and evaluation strategies for oncolytic virus ★ Experience about R&D, transformation of gene therapy ★ R&D, druggability and application of therapeutic vaccines | Who would attend: ★ Management of biopharmaceutical and biotechnology companies: Head of early R&D, mechanism research, drug discovery, project survey and setting up department ★ PI from Universities, research institutions and hospitals: Scientist majored in pharmacy, translational medicine, biology and life science |
Oncolytic Virus CMC Research | |
What you will learn: ★ Technical requirements for quality control of gene therapy according to latest pharmacopoeia ★ New methods for oncolytic virus CMC and impurity analysis identification and control to accelerate IND ★ Best practice for upstream culture and downstream purification of oncolytic virus ★ Aspetic productive process of virus therapy products | Who would attend: ★ Head of quality research and analysis, process development and pharmacy administration department from oncolytic virus and gene therapy companies ★ Head of process development, manufacturing, technology, quality analysis department form CDMO working on virus |
Design of Clinical Trials and Quality Management of Biopharma | |
What you will learn: ★ Preclinical drug evaluation and accurate targets verification ★ Research on innovative animal evaluation model and efficacy evaluation ★ Global synchronous clinical R&D strategy and scheme design ★ Regulatory guide for combination therapy and its latest progress | Who would attend: ★ Head of clinical R&D, pharmacology, toxicology, clinical R&D, clinical medicine department from biopharmaceutical companies ★ Head of RA department from biopharmaceutical companies ★ PI from clinical trial organization and doctors majored in related indications |
BioProcess Improvement and Change Management / BioProcess Characterization and Validation | |
What you will learn: ★ Latest interpretation of global guide for biotechnology process change ★ Latest requirements of batch change, raw material, equipment, packaging material, technology for post-marketed biologics ★ Experience of improvement and change for biologics process ★ Characterization and continuous verification strategies for process of biologics | Who would attend: ★ Head of optimization and amplification process department ★ Head of technological transfer department ★ Head of upstream and downstream process development department ★ Head of registration and application department |
Novel Antibody Quality Characterization and Analysis | |
What you will learn: ★ Characterization and analysis of new complex antibody ★ Characterization of antibody by cutting-edge detection technologies ★ Quality analysis and control methods for residues during biopharmaceutical process ★ Construction and management experience of key quality system for the R&D and release of new biologics | Who would attend: ★ Head of quality analysis, analysis science department ★ Head of production and QA/QC department |