“药物非临床研究质量管理规范”的概念、定义、翻译、参考文献-科学参考

单词	药物非临床研究质量管理规范
释义	药物非临床研究质量管理规范 Encyclopedia 医学药物非临床研究质量管理规范释 Good Laboratory Practice for non-clinical laboratory studies; GLP药物非临床研究质量管理规范由国家药品监督管理局（National Medical Products Administration; NMPA）根据《中华人民共和国药品管理法》《中华人民共和国药品管理法实施条例》制定并发布，旨在提高药品非临床研究的质量，确保实验资料的真实性、完整性和可靠性，保障人民用药安全的规定。
随便看	underground granary underground gravity survey underground haulage machinery underground health facilities underground high pressure operation safety underground hydropower station underground in pit tank underground intelligent pipe network underground launching silo underground leaching of ore underground loading equipment underground logistics system planning underground magnetic resonance imaging system underground material transpoter underground mechanized scaler underground mine development underground mine development choice underground mined-out areas underground mine emergency refuge system underground mine intelligent dispatch underground mining construction schedule planning underground mining machinery underground mining methods underground mining schedule planning underground multifunctional vehicle

科学参考收录了854744条科技类词条，基本涵盖了常见科技类参考文献及英语词汇的翻译，是科学学习和研究的有利工具。