为了提高药品安全性研究的质量,并与国际研究规范接轨,中华人民共和国国家科学技术委员会发布了《药品非临床研究质量管理规定》(国际通称GLP)。国家医药管理局在提出加强新药研究工作的同时,十分重视制定和推行我国的GLP。为提高医药行业的GLP意识,国家医药管理局将组织有关专家编写实施指南, In order to improve the quality of drug safety research and to conform to international research standards, the National Science and Technology Commission of the People’s Republic of China promulgated the “Regulations on the Quality Management of Non-clinical Drug Research” (GLP International). While proposing to strengthen the research on new drugs, the State Pharmaceutical Administration attaches great importance to the formulation and implementation of GLP in our country. To enhance GLP awareness in the pharmaceutical industry, the State Pharmaceutical Administration will organize relevant experts to prepare implementation guidelines,