Su Shengfeng made a report entitled "Committed to Reform, Creating Dual Districts—Specific Practice of Comprehensive Reform of Drug Supervision in Guangdong Province". He said that the high-quality development of the industry is inseparable from the new pattern of social governance of co-construction, co-governance, and sharing. After in-depth analysis and serious thinking, the Provincial Food and Drug Administration put forward the strategic thinking and work goals of "holding high the banner of comprehensive reform of drug supervision and building a national drug quality and safety demonstration zone and a national drug industry high-quality development demonstration zone" based on the actual situation in Guangdong. Specific tasks include the issuance of the "Guangdong Province Drug Safety Responsibility Assessment Program", the establishment of a national vaccine regulatory system assessment and vaccine regulatory quality management system construction, the formulation and promulgation of the "Provincial Administration Drug Comprehensive Reform Project Management Measures", and the formulation and implementation of the "Key Projects of Biomedicine Industry, Measures for the Administration of Innovative Services in Key Enterprises and Key Regions (for Trial Implementation), introduced and implemented the “Guangdong-Hong Kong-Macao Greater Bay Area Pharmaceutical and Medical Device Regulatory Innovation and Development Work Plan”, “Guangdong Province’s Implementation Plan for Promoting the High-quality Development of the Cosmetics Industry”, and formulated “Professional Professionalization” The “Implementation Plan for Building a Team of Drug Inspectors” and a series of supporting systems, and actively promote the evaluation of the national vaccine regulatory system.