domain
Pharmaceutical
(5 standards)Industries: Pharmaceutical
GMP (cGMP)Active
GMP (cGMP)
Good Manufacturing Practice — WHO Guidelines & FDA 21 CFR 210/211
GlobalUnited States
ICH E6(R3)Final ICH Step 4 — regional implementation varies
ICH E6(R3)
Good Clinical Practice for clinical trials involving human participants
GlobalEuropean UnionUnited StatesUnited KingdomCanadaJapanChina
ISO 37301:2021Active
ISO 37301:2021
Compliance management systems — Requirements with guidance for use
Global
ISO 35001:2019Active
ISO 35001:2019
Biorisk management for laboratories and other related organisations
Global
EU CLP RegulationActive
EU CLP Regulation
Classification, Labelling and Packaging of Substances and Mixtures — Regulation (EC) No 1272/2008
European UnionEuropean Economic Area