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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。
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aquatic product raw material handling machinery
aquatic product refrigerating technology
aquatic products agent
aquatic products biologic hazards
aquatic products canning technology
aquatic products chemical detection technology
aquatic products chemistry
aquatic products chill storage logistic
aquatic products circulation
aquatic products detection technology
aquatic products dietary toxicant
aquatic products drying technology
aquatic products foodborne parasites
aquatic products foodborne pathogens
aquatic products frozen storage logistics
aquatic products lipid
aquatic product smoking equipment
aquatic products polysaccharide
aquatic products preservation
aquatic products processing and trade of China
aquatic products processing machinery
Aquatic Products Processing Technology
aquatic products risk management
aquatic products sensory evaluation
aquatic products traceability technology
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更新时间:2026/7/20 7:00:46