The drug inspection competence of pharmaceutical corporations in China is now in part at a low level, so it can be efficiently improved by participating in the laboratory accreditation.
我国药品生产企业部分检验实验室管理水平低下，参与实验室认可，可有效地提升企业的检验能力。
Study inspection of preclinical safety evaluation of drug is an important responsibility for quality assurance unit (QAU) with good laboratory practice (GLP).
对新药安全性实验实施质量监督检查是药物非临床研究质量管理规范(GLP)赋予质量保证部门(QAU)的重要职责。
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