GMP
(Kev Tsim Khoom Zoo Rau Tshuaj)
CGMP
(Cov kev coj ua zoo tam sim no)
ICH
(International Conference on Harmonization of Technical Requirements for Register of Pharmaceuticals for Tib neeg siv)
FDA
(Food and Drug Administration)
NMPA
(National Medical Products Administration)
CDE
(Center for Drug Evaluation)
EDQM
(European Directorate for The Quality of Medicines)
MHRA
(Lub Chaw Haujlwm Saib Xyuas Kev Noj Qab Haus Huv thiab Tshuaj Kho Mob)
WHO
(Koom Haum Saib Xyuas Kev Noj Qab Haus Huv Thoob Ntiaj Teb)
PIC/S
(Kev Tshawb Fawb Kev Tshawb Fawb Kev Tshawb Fawb thiab Kev Tshawb Fawb Kev Tshawb Fawb Kev Lag Luam)
DMF
(Drug Master File)
CEP
(Certificate of Suitability to Monograph of European Pharmacopeia)
ASMF
(Active Substance Master File)
EIR
(Daim Ntawv Qhia Kev Tshawb Fawb Txog Kev Tsim Kho)
VMP
(Validate Master Plan)
Post lub sij hawm: Feb-18-2022