Sichuan Deebio Pharmaceutical Co., Ltd yakagamuchira ongororo yeGMP yepamutemo kubva kuJapan PMDA kubva pa8.25 kusvika 8.26 muna 2022. Chikwata chekuongorora cheGMP chaisanganisira vaongorori vaviri vachitungamirirwa nenyanzvi dzakagara nebasa uye vakaita ongororo yemazuva maviri iri kure.Nyanzvi dzechikwata chekuongorora dzakaita ongororo yakazara yeDeebio's quality management system, production management system, pa-saiti mashandiro, manejimendi emurabhoritari, zvivakwa zvinotsigira zvine chekuita nemidziyo, uye kuchengetedza masisitimu everuzhinji.
 
Kuburikidza nekuongorora uku, nyanzvi dzechikwata chekuongorora dzakatsigira pamwe uye dzakaziva zvakanyanya Deebio's GMP mhando yekutonga system.Pakupedzisira, Deebio akabudirira kupasa zviri pamutemo GMP certification yeJapan PMDA!

PMDA (Pharmaceuticals and Medical Devices Agency) isangano reJapan rinoona nezvekuongorora kwehunyanzvi kwemishonga nemidziyo yekurapa.Inoshanda zvakafanana neFDA muUnited States uye NMPA muChina.

Deebio akapasa EU-GMP uye Chinese GMP certification.Kupasa kwakabudirira kwechitupa chePMDA cheJapan kunoratidza kukunda kwechikamu muhurongwa hwepasi rose hwaDeebio!