In order to promote the capacity of inspectorate, and continuously improve the professional skills and comprehensive quality of the inspectors, CFDI held the second experts’ forum on March 18th, 2021. Sun Huimin, director of the Verification Institute of Packaging Materials and Pharmaceutical Excipients, National Institutes for Food and Drug Control, was invited and gave a lecture with the topic of "Risk and Control of Pharmaceutical Packaging Materials".

Director Sun introduced the definition, development and supervision history, industry overview and other basic information of pharmaceutical packaging materials, detailed explained the regulatory requirements, test standards and quality risk cases, and also shared the compatibility study and inspection points of pharmaceutical packaging materials . Director Sun’s lecture was comprehensive and detailed, with rich examples, allowing the inspectors systematically understand the knowledge of pharmaceutical packaging materials, and have important guiding and reference value for the Supervision and inspection of pharmaceutical packaging materials .

Sun Huimin, the current director of the Verification Institute of Packaging Materials and Pharmaceutical Excipients, National Institutes for Food and Drug Control, also the director of the Key Laboratory of Quality Research and Evaluation of Pharmaceutical Excipients of NMPA. Over the years, he has been engaged in the work of drug verification, standard review of imported drugs, quality control and safety risk assessment of pharmaceutical excipients and pharmaceutical packaging materials, and formulation of guiding principles for the registration and evaluation of pharmaceutical packaging materials.

CFDI, Yangtze River Delta sub center for drug evaluation and inspection ofNMPA and 27 provincial drugs inspectorates synchronously watching through video system participated in the training; totally more than 560 people participated in the training.