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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
drug manufacturer
drug metabolism
drug metabolizing enzymes analysis
drug moxa stick
drug nomenclature
drug non-clinical pharmacodynamics research
drug physical stability testing
drug physiological stability testing
drug-plasma protein binding study
drug poisoning
drug pool's management system
drug pre-treatment by ultrafiltration technology
drug pretreatment techniques for equilibrium dialysis method
drug prevention
drug pricing management
drug protection
drug provision and security system
drug quality
drug rapid inspection
drug raw materials testing
Drug-Receptor Interaction Theory
drug reevaluation
drug rehabilitation
drug resistant gene
drug resistant strain
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