Leong Goh

Leong Goh is Quality Management professional with over 20 years in various areas; from small molecule, cell therapy products to traditional biologics. He worked with New Zealand’s Ministry of Health medicines and medical devices regulatory authority (MEDSAFE) performing GMP inspections and product assessments. He had worked with several Chinese medicine manufacturers and successfully hosted GMP inspections that resulted in product approvals from several countries including Europe and USA. He has a Master in Medical Science (Drug Development) from University of New South Wales (Australia) and a Master in Biochemistry Massey University (New Zealand).