摘要
综述了对最终灭菌产品的无菌质量评价实行参数放行的理论基础和实践要求 。
The theoretic bases and practice requirements of implementing parametric release for the quality evaluation of the terminal sterilized products were described. The meaning and prospect about implementing parametric release were also discussed.
出处
《中国医药工业杂志》
CAS
CSCD
北大核心
2003年第6期299-301,共3页
Chinese Journal of Pharmaceuticals
关键词
最终灭菌产品
无菌
参数放行
terminally sterilized products
sterility
parametric release
