场地管理文件可以参考如下:
1、EUROPEAN MEDICINES AGENCY--Guideline on Active Substance Master File Procedure( November 2018);
2、EUROPEAN COMMISSION--EudraLex The Rules Governing Medicinal Products in the European Union Volume 4 Good Manufacturing Practice Medicinal Products for Human and Veterinary Use Explanatory Notes on the preparation of a Site Master File
3、EUROPEAN MEDICINES AGENCY--Active Substance Master File (ASMF) worksharing procedure Submitting an initial worksharing ASMF
4、国家药品监督管理局的药品生产场地管理文件指南(试行)-征求意见稿(2020.12)
5、湖北省药品生产场地管理文件编制指南(征求意见稿)