摘要
GLP是国际通行的药品非临床试验质量管理规范 ,实施过程中 ,在整备合格的硬件设施前提下 ,应该加强GLP组织体制、GLP意识。
GLP is a current international standard for non-clinic al laboratory study. During the implementation, based on qualified hardware, we sh ould strengthen organization system, set up awareness and stress quality managem ent.
出处
《中国药事》
CAS
2004年第3期168-169,共2页
Chinese Pharmaceutical Affairs