摘要
药品质量检测结果的可靠性可从生产、加工、检测、运输和保存等多方面进行阐述辨析,启示药品质检的可靠性要从根本上进行约束,从生产方面进行制约;其次,要提高科学技术水平,完善药品质量检测的专属性;最后,增强质检人员的服务意识,坚持有法必依,按照标准进行检测,为质量检测可靠性提供保障。
Drug quality reliability of test results from the production, processing, testing, transportation, preservation, and many other elaborate discrimination, constraints revelation Drug Quality reliability fundamentally, be restricted from production; Second, we must improve our scientific technical level, thus improving the specificity of drug quality testing; and finally, enhance awareness of service quality staff, adhere to the law must, in accordance with the standards for testing, quality testing to provide protection reliability.
出处
《生物化工》
2016年第2期74-76,共3页
Biological Chemical Engineering
关键词
药品质量
质量监管
控制分析
Drug quality
Quality control
Control analysis