World Health Organ Tech Rep Ser. 2014(986):1-387, back cover.
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, in addition to 20 monographs and general texts for inclusion in The International Pharmacopoeia and 11 new International Chemical Reference Substances. The International Pharmacopoeia--updating mechanism for the section on radiopharmaceuticals; WHO good manufacturing practices for pharmaceutical products: main principles; Model quality assurance system for procurement agencies; Assessment tool based on the model quality assurance system for procurement agencies: aide-memoire for inspection; Guidelines on submission of documentation for prequalification of finished pharmaceutical products approved by stringent regulatory authorities; and Guidelines on submission of documentation for a multisource (generic) finished pharmaceutical product: quality part.
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和国际共识达成程序来制定标准。除了20篇专论和通用文本将纳入《国际药典》以及11种新的国际化学参考物质外,还通过并推荐使用以下新指南:《国际药典》——放射性药物章节的更新机制;世界卫生组织药品生产质量管理规范:主要原则;采购机构的模范质量保证体系;基于采购机构模范质量保证体系的评估工具:检查备忘;由严格监管当局批准的成品药品预认证文件提交指南;以及多来源(仿制药)成品药品文件提交指南:质量部分。