论文部分内容阅读
根据国家食品药品监督管理总局发布《药品医疗器械飞行检查办法》的规定,将药品和医疗器械研制、生产、经营和使用全过程纳入飞行检查的范围,将于2015年9月1日起施行。对被检查单位“拒绝、逃避监督检查”等不配合情形,将按照有关规定从重处罚。据了解,所谓飞行检查,是食药监管部门针对行政相对人开展的不预先告知的监督检查,具有突击性、独立性、高效性等特点。飞行检查是一种十分有效的检查办法,在调查问题、管控风险、震慑违法行为等方面发
According to the regulations issued by the State Food and Drug Administration on the Medical Inspection Procedures for Medical Devices, the entire process of research, production, operation and use of pharmaceuticals and medical devices will be included in the scope of flight inspection and will come into effect on September 1, 2015. The unit under inspection “refuse, evade supervision and inspection ” and other non-cooperation situations will be severely punished in accordance with the relevant provisions. It is understood that the so-called flight check, is the food and drug regulatory authorities for the implementation of the relevant administrative non-prioritized supervision and inspection, with the characteristics of surprise, independence, and efficiency. Flight inspection is a very effective inspection method, in the investigation of issues, risk management, deterring illegal activities, etc.