Sichuan Deebio Pharmaceutical Co., Ltd nabatara nyocha nnabata GMP gọọmentị sitere na Japan PMDA site na 8.25 ruo 8.26 na 2022. Ndị otu nyocha GMP nwere ndị nyocha abụọ nke ndị ọkachamara nwere ahụmahụ na-ahụ maka agha na-eduzi wee mee nyocha anya ụbọchị abụọ.Ndị ọkachamara nke ndị ọrụ nyocha ahụ mere nyocha zuru oke nke usoro nlekọta àgwà nke Deebio, usoro nhazi mmepụta ihe, ọrụ na saịtị, njikwa ụlọ nyocha, ihe ndị na-akwado ihe ndị metụtara ya na akụrụngwa, na nhazi nke usoro ọha.
 
Site na nyocha a, ndị ọkachamara nke otu nleba anya ekwupụtala n'otu n'otu ma ghọta nke ọma usoro njikwa ogo GMP nke Deebio.N'ikpeazụ, Deebio agafeela asambodo GMP gọọmentị nke PMDA nke Japan!

PMDA (ụlọ ọrụ ọgwụ na ngwaọrụ ahụike) bụ ụlọ ọrụ Japan na-ahụ maka nyocha teknụzụ nke ọgwụ na ngwaọrụ ahụike.Ọ na-arụ ọrụ yiri FDA na United States na NMPA na China.

Deebio agafeela asambodo EU-GMP na Chinese GMP.Ngafe asambodo PMDA nke Japan na-aga nke ọma bụ akara mmeri na atụmatụ zuru ụwa ọnụ nke Deebio!