各位坛友,有没有了解《WHO Technical Report Series No. 957 Annex 5 2010 Good Distribution Practice》 的,请教2个问题:
1、WHO Technical Report Series No. 957 Annex 5 2010 Good Distribution Practice 7里面有没有规定药品仓库的进货和出货不能用同一个门?
2、WHO Technical Report Series No. 957 Annex 5 2010 Good Distribution Practice 13里面有没有规定进行药品包装过程中的质量检查的抽样数量必须遵循什么规则?