目前,制药企业是否通过GMP,作为企业生存的条件。医疗机构制剂室以是否通过GPP,作为制剂室生存的条件。国家药品监督管理局通过对药品生产、流通、经营、使用等环节的层层管理加强药品的监督管理。保证人民用药安全,近来,《中国医药经济报》2001年2月第12期对医院临床静脉输液配液需作净化提出要求,本人作为一名药学工作者对医院临床输液配制提自己的几点看法。1医院临床输液配制未作空气净化,不能保障人民用药安 At present, whether pharmaceutical companies pass GMP is the condition for their survival. Medical institutions preparation room to pass GPP, as a preparation room survival conditions. The State Drug Administration strengthens the supervision and administration of drugs through various layers of management including drug production, circulation, operation and use. Recently, the “Chinese Medical and Economic News” No. 12 in February 2001 on the clinical venous infusion solution to be purified hospital requirements, as a pharmacy workers on the hospital clinical infusion preparation of their own points view. 1 hospital clinical infusion preparation is not for air purification, can not protect people's medication safety