domain
制药
(3 项标准)行业: 制药
GMP (cGMP)Active
GMP (cGMP)
Good Manufacturing Practice — WHO Guidelines & FDA 21 CFR 210/211
全球美国
ISO 37301:2021Active
ISO 37301:2021
Compliance management systems — Requirements with guidance for use
全球
EU CLP RegulationActive
EU CLP Regulation
Classification, Labelling and Packaging of Substances and Mixtures — Regulation (EC) No 1272/2008
欧盟欧洲经济区