The Trainer has over 25 years of experience in the pharmaceutical and medical device industry and has worked in the industry in China, New Zealand, Australia, Singapore and other ASEAN countries. He has held senior positions in the areas of Quality Assurance, Regulatory Compliance and Regulatory Affairs and has been responsible for maintenance of regulatory compliance of active ingredient manufacturer’s drug master files (DMF) and European certificates of suitability (CEPs).

Not only The Trainer has extensive analytical testing and quality control experience, production engineering experience involving trouble shooting, process optimization and long-term process/ product development activities, he also has experience in GMP compliance auditing while employed by China State Food and Drug Administration (CFDA). In this role, The Trainer conducted for regulatory audits to Chinese pharmaceutical company within mainland China. Following his professional experiences at CFDA, Pacific Pharmaceuticals (New Zealand, now Merck Group), Go Medical Industries (Australia), Wyeth (Singapore, now Pfizer). He is currently a principal consultant in ChemPharm, and leading consultant team to participate GMP/ GLP/GDP/GVP projects in mainland China, Hong Kong, Taiwan, Australia, New Zealand and ASEAN countries.

The Trainer has a wealth of knowledge in regulatory compliance, validations, project management, GMP/GLP/GDP/GVP and regulatory affairs, he has designed and conducted series of GxP training courses to train thousands of industries professional. Chuan was a Drug Abuse Inspector with the China Drug Control Center, Beij ing, China and was appointed to the position of a drug inspector at the Beijing 11th Asian Games in which he was awarded an Honorary Diploma from the Olympic Committee. Chuan The Trainer is fluent in both English and Chinese.