Suppr超能文献

世界卫生组织药品制剂规范专家委员会

WHO Expert Committee on Specifications for Pharmaceutical Preparations.

出版信息

World Health Organ Tech Rep Ser. 2012(970):1-235, back cover.

Abstract

The Expert Committee on Specifications for Pharmaceutical Preparations works towards clear, independent and practical standards and guidelines for the quality assurance of medicines. Standards are developed by the Committee through worldwide consultation and an international consensus-building process. The following new guidelines were adopted and recommended for use: Development of monographs for The International Pharmacopoeia; WHO good manufacturing practices: water for pharmaceutical use; Pharmaceutical development of multisource (generic) pharmaceutical products--points to consider; Guidelines on submission of documentation for a multisource (generic) finished pharmaceutical product for the WHO Prequalification of Medicines Programme: quality part; Development of paediatric medicines: points to consider in formulation; Recommendations for quality requirements for artemisinin as a starting material in the production of antimalarial active pharmaceutical ingredients.

摘要

药品制剂规范专家委员会致力于制定清晰、独立且实用的药品质量保证标准和指南。委员会通过全球范围内的磋商以及国际共识达成过程来制定标准。以下新指南已获采纳并建议使用:《国际药典》各论的制定;世卫组织药品生产质量管理规范:药用用水;多源(仿制药)药品的药学开发——需考虑的要点;向世卫组织药品预认证计划提交多源(仿制药)成品药文件的指南:质量部分;儿科药品的开发:制剂方面需考虑的要点;关于青蒿素作为抗疟活性药物成分生产起始原料的质量要求建议。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验