药品包装用材料、容器注册工作程序一、Ⅰ类药包材的初审1、生产Ⅰ类药包材的企业应填写《药品包装用材料、容器申请表》连同要求提交的资料一式 4份及样品交市级药品监管局预审后集中报省药品监管局。2、省药品监管局对Ⅰ类药包材申报资料进行审查 ,申报资料不齐全的 ,退还申 Pharmaceutical packaging materials, container registration procedures A class Ⅰ drug packaging materials of the first instance 1, the production of Class Ⅰ drug packaging materials enterprises should fill out the “drug packaging materials, containers application form” together with the required information submitted in quadruplicate and the sample After the pre-trial municipal and municipal drug regulatory focus on the provincial Drug Administration. 2, the provincial Drug Administration to review the class I drug package materials to declare the information is not complete, refund