8European Commission EudraLex: the rules governing medicinal products in the European Union. EU guidelines to good manufacturing practices, medicinal products for human and veterinary use[ S]. Brussels : EC,2005. 被引量:1
9European Commission EC. administrative procedure official control authority batch release[ S]. Brussels:E C.2001. 被引量:1
10The European Agency for the Evaluation of Medicinal Products. Medicinal products GMP inspection and batch certification[ S]. London:The European Agency for the Evaluation of Medicinal Products Inspections ,2003. 被引量:1