Zou Yong，Independent Consultant, CB Consultant(Beijing) Ltd.

Topic: From GMP to Quality Management System Cover Full Pharmaceutical Life cycle

 Speaker Bio

Mr. ZOU graduated from the department of chemistry of Peking University and went to the National University of Singapore for his master's degree. Mr. ZOU has nearly 20 years of working experience in the pharmaceutical industry, successively engaged in R&D, production management and quality management, including different areas such as chemical drugs, Chinese Traditional Drugs, biological products and cell therapy. He has led the company to pass a series of international certifications, such as WHO PQ. Mr. ZOU now is mainly engaged in quality management consultation for pharmaceutical companies, including GMP, quality management system, quality risk management, qualification and validation, international GMP certification, quality management tools (deviation, CAPA, change, etc.), single-use system, vaccine production,

etc. Since 2017, he has been employed as a GMP consultant by Beijing NMPA. 

Presentation Summary

1. Changes in the requirements of external regulations

2. Enterprise's self-development needs

3. How to implement full life cycle quality management