Topic：Regulatory Trends for Cleaning Validation of Small Molecule Drugs        

Qu Manhong, Senior Engineer and licensed pharmacist, graduated from Shandong Medical University (now Shandong University), majoring in pharmacy. Now working in the Pharmacovigilance Department of Shandong Anxin Pharmaceutical Co., LTD., Qilu Pharmaceutical Group. Before that, Qu Manhong was in charge of supplier management department, Quality assurance Department, preparation park quality management Department and other production quality management of Qilu Pharmaceutical Co., LTD. During more than 20 years’ management of pharmaceutical production quality and the experience of working with domestic and foreign official audits, Qu Manhong is familiar with the requirements and technical guidelines for drugs of GMP of Europe, America, China, Japan and other countries, and has rich experience in pharmaceutical production quality management and supplier management; Qu manhong has audit on hundreds of suppliers of raw materials, packaging materials, and pharmaceutical intermediates, and assist supplier to improve production management level, ensuring the safety of production materials. As a trainer, Qu Manhong have made many speeches at the invitation of National Biological Industry Conference, PDI, CPAPE, and China Pharmaceutical Auxiliary Materials Development Alliance, etc.