In the past few days, the Dongxiang County Market Supervision and Administration Bureau has continued to deepen the consolidation and improvement of drug safety in accordance with the annual supervision and inspection plan, fully implemented the "four strictest" requirements, strictly prevented, strictly controlled and strictly managed drug safety risks, and built a solid bottom line of drug safety in an all-round way.
Implement the main responsibility and strengthen closed-loop control. Print and distribute the key points of the annual drug circulation supervision and medical device supervision, refine the annual "two products and one device" supervision task, conduct pressure layer by layer, implement it to the people, strengthen the whole chain, the whole process before, during, and after the event, and the integrated supervision of online and offline, so as to build a complete chain of responsibility and supervision network. Focus on key varieties, regions and links, in-depth investigation of safety risks and hidden dangers, real-time monitoring and early warning, dynamic assessment and control, and promote the transformation of drug safety from "passive defense" to "active prevention and control".
Based on daily supervision, strengthen risk investigation. Focus on key business entities, combine routine inspections with daily inspections, continue to focus on key units such as urban-rural interfaces, rural pharmacies, and private medical institutions, and comprehensively investigate risks and hidden dangers through inspection and verification, supervision and sampling, adverse reaction monitoring, online sales monitoring, complaints and reports, public opinion monitoring and other means.
Improve long-term mechanisms, scientifically standardize supervision. Implement hierarchical and classified drug supervision, follow the rules of drug supervision, improve and improve regulatory credit files, and ensure the orderly connection of drug supervision before, during and after the event; Promote the hierarchical supervision of medical device operation, carry out "targeted" supervision and inspection in accordance with the principle of "risk classification, scientific supervision, comprehensive coverage, dynamic adjustment, implementation of responsibility, and improvement of efficiency", give full play to the technical support role of drug supervision and sampling, fully grasp the quality status of drugs, take the initiative to find hidden problems, and prevent and control safety risks in a timely manner.
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Written by: Ma Kaili
Editor: Zhang Yu
Proofreading: Ma Jinlong
Review: Qi Zhengli