GMP
Bene Vestibulum Practice enim medicamentis
CGMP
Current Bene Fabrica Exercitia）
ICH
International Conference on Harmonization of Technical Requirements for Registration Pharmaceuticals for Human Use）
FDA
Cibus et medicamentis Administration）
NMPA
National Medical Products Administration）
CDE
Center enim medicamentis Aestimatio
EDQM
European Directorate pro Medicinae qualitate
MHRA
Medicina et curis Products Regulatory Agency）
OMS
(Ordo Mundi Sanitarius)
PIC/S
Pharmaceutical Inspectio Convention and Pharmaceutical Inspection Cooperation Scheme）
DMF
Drug Magister File）
CEP
Certificatio idoneitatis ad Monographum Pharmacopaeae Europaeae
ASMF
Activae Substantiae Magister File）
EIR
Estitatio recognitionis Report）
VMP
Validate Magister Plan）
Post tempus: Feb-18-2022