摘要
结合笔者设计案例介绍在《药品生产质量管理规范》(2010年修订)要求下,对无菌冻干粉针剂车间的净化空调系统的设计过程和应注意的问题。
With the author design case described in the "drug production quality management standards" (2010 Revision) requirement, the design process of purifying air conditioning system sterile freeze-dried powder injection workshop and problems should be paid attention to.
出处
《广东化工》
CAS
2013年第22期109-110,共2页
Guangdong Chemical Industry
关键词
净化空调系统
粉针剂
局部A级
clean air-conditioning systems
injection products
Local Grade A