Develop, implement and maintain standard policies, procedures (SOPs) and controlled (GMP) document systems in compliance with current good manufacturing practice regulations.

制定，实施和维护标准的政策，程序（标准操作程序）和控制（的GMP ）的文件系统符合现行优良制造规范条例。

Drug manufacturers shall conduct production according to the Good Manufacturing Practice Products (GMP) formulated by the drug regulatory agency of the State Council based on this Law.

药品生产企业必须按照国务院药品监督管理部门依据本法制定的《药品生产质量管理规范》组织生产。