(5) a drug manufacturer that conducts repackaging shall hold the Drug Manufacturing Certificate. To apply for repackaging of import unpackaged tablets and capsules, the manufacturer shall also hold the GMP certificate covering the dosage forms for repackaging; and (6) An application for drug repackagi...
Since China's State Food and Drug Administration (SFDA) revised its GMPs last year (they became effective Mar. 1, 2011), the agency has been making other improvements to enhance the quality of its pharmaceutical manufacturing industry. Many improvements are tied to the...
药品生产企 … manage.cas.cn|基于1952个网页 3. 中国食品药品监督管理局 搜索中国食品药品监督管理局(SFDA)里面可以搜到生产许可证!|评论 "施慧达"是药品的商品名,本药品的通用名叫“苯磺酸 … zhidao.baidu.com|基于996个网页 更多释义 例句
Certain products, such as pharmaceuticals, undergo additional layers of scrutiny. These can include departmental meetings, laboratory testing, Good Manufacturing Practice (GMP) inspections, pricing committee evaluations, and final approval by the main drug committee. ...
GMP critical computerised systems 与药品生产质量相关的关键计算机化系统 - Description of GMP critical computerised systems (excluding equipment specific Programmable Logic Controllers (PLCs)). 简述与药品生产质量相关的关键的计算机化系统情况(不包括逻辑编程器(PLCs))。 Documentation 文件 Description of ...