《国家食品药品安全“十一五”规划》将加快信息化建设作为保障人民群众健康安全、提升监管能力建设的重要内容。党中央、国务院对食品药品监管信息化建设提出了明确要求,中央领导多次指示要切实加强药品研制、生产、流通、使用全过程的监管,加快信息化建设,建立健全审评、审批权力的内外部监管监督制约机制。因此,制药企业逐渐采用药品质量监控及安全追溯管理解决方案,借助全面完整的信息管理监 The State Food and Drug Safety Eleventh Five-Year Plan will speed up the construction of informatization as an important part of safeguarding the people’s health and safety and enhancing the regulatory capacity. The Central Party Committee and the State Council set forth clear requirements on the informatization of food and drug administration. The central leadership has repeatedly instructed that the entire process of drug development, production, circulation and use should be supervised to speed up the construction of informatization and establish a sound review and approval authority Internal and external supervision, supervision and control mechanism. Therefore, pharmaceutical companies gradually adopt drug quality control and traceability management solutions, with a full and complete information management supervision