He Hoa Hilinaʻi

Loaʻa iā Conlight Medical kahi hale hana GMP e hana ana i nā mea hana a me nā reagents in vitro. Ua hala ia i ka palapala hōʻoia ISO 13485 a me Medical Device Single Audit Program (MDSAP) e ka British Standards Institution BSI) a he mau mana lako paʻa ikaika.

I kēia manawa, ua kūkulu ʻia he 8 mau laina hana o nā reagents diagnostic in vitro a me nā mea lapaʻau, me ka mana i hoʻolālā ʻia he 15 miliona mau ʻāpana/makahiki a me ka waiwai hana a hiki i ka 5 biliona yuan/makahiki. I ka manawa like, loaʻa iā ia ka palapala Sila Nui PCT honua mua no nā pahu hoʻāʻo olakino ma Kina a ʻoi aku ma mua o 50 mau pahu hoʻāʻo i hōʻoia ʻia e EU.