Sichuan Deebio Pharmaceutical Co., Ltd idavomereza kuyendera kovomerezeka kwa GMP kuchokera ku Japan PMDA kuchokera pa 8.25 mpaka 8.26 mu 2022. Gulu lofufuza za GMP linali ndi ofufuza awiri otsogozedwa ndi akatswiri odziwa ntchito zakale ndipo adachita kafukufuku wamasiku awiri wakutali.Akatswiri a gulu loyang'anira adayang'ana mozama za kayendetsedwe kabwino ka Deebio, kasamalidwe kazinthu, kasamalidwe ka malo, kasamalidwe ka labotale, zida zothandizira ndi zida, komanso kukonza machitidwe aboma.
 
Kupyolera mu kuyenderako, akatswiri a gulu loyendera atsimikizira ndikugwirizana kwambiri ndi Deebio's GMP management management system.Pomaliza, Deebio adapambana chiphaso cha GMP cha PMDA yaku Japan!

PMDA (Pharmaceuticals and Medical Devices Agency) ndi bungwe la ku Japan lomwe limayang'anira kuwunika kwaukadaulo kwamankhwala ndi zida zamankhwala.Zimagwira ntchito mofanana ndi FDA ku United States ndi NMPA ku China.

Deebio wadutsa EU-GMP ndi Chinese GMP certification.Kupambana kopambana kwa satifiketi ya PMDA yaku Japan kukuwonetsa kupambana pang'onopang'ono munjira yapadziko lonse ya Deebio!