Pono nā huahana maikaʻi kiʻekiʻe
nā hiʻohiʻona maikaʻi
ʻO mākou kā mākou huahana ʻo GMP, cGMP
ISO : 9001: 2008 i hōʻoia ʻia.
Hāʻawi mākou i ko CMO & API i ka hoʻokahi hoʻokahi-mālama
nā hua'ōlelo: R&D, hana hana, hana hoʻōla-
kuai a me ke kuai.

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ʻO kā mākouʻoihana

Hoʻohana ʻo CMO a me API

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Ke kuhi a me kaʻaelike R & D

Hiki i ka CMOAPI ke hāʻawi i nā lawelawe i hala, nā mea a pau i kākoʻo ʻia e kā mākou mau kuleana koʻikoʻi ma ka pale ʻana i ka naʻau o Intellectual Property (IP), e hōʻoia ana e mālama ʻia nā hana ma ke koʻikoʻi o ka hilinaʻi i nā manawa āpau.

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Ka liʻiliʻi liʻiliʻi a me kaʻoihana nui

No nā makahiki he ʻumi i hala aku nei, ua hoʻolako ʻo CMOAPI i nā synt synthes maʻamau a me nā lawelawe hana. Hiki i kā mākou lawelawe lawelawe mai ka pahu liʻiliʻi liʻiliʻi o milligram a hiki i nā tonona hana nui.

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Ke kūkuluʻana i nā papa no kaʻike lāʻau

ʻO CMOAPI no ka Drug Discovery he kapua, kūlou a me ka hopohopo e nānā ana i ka ʻike ʻepekema a me ka ʻikepili e hōʻike i nā ʻike ʻike a huna ʻia e hiki ke kōkua i ka hoʻonui ʻana i ka hopena ʻepekema kūpilikiʻi.

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Hoʻomaka R & D a me ka hoʻolālā hou

ʻO kā mākou papa hana hoʻolālāʻokoʻa, iʻoi aku ka nui o nā mea'elekema o ka 50 ma ko mākou mau'āina,ʻoi aʻe ma mua o nā manaʻo ma nā papahanaʻoihana paʻakikī loa. Ke hana nei i loko o nā laboratories o ka moku'āina o nāʻoihana i hoʻolakoʻia me ka mea hana hou loa a me nā meaʻimi kākau.

E PILI ANA IĀ MĀKOU

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He mea hoʻolako ʻo CMOAPI i kahi mea lapaʻau maʻamau synt syntical a me ke aelike R&D.

JINAN CMOAPI BIOTECHNOLOGY CO., LIMITED. hoʻokumu ʻia i 2007, kahi hui ʻoihana ʻenehana i komo i ka ʻimi noiʻi, hoʻomohala ʻana a me ka kūʻai aku ʻana i ka huahana pharmaceutical raw materials.The hualy hua ʻowi a: Lorcaserin, nā kikowaena o Lorcaserin, orlistat , Sesamol, tadalafil a me nā waena o tadalafil, etc.

Mālama ko mākou hale hana mea ʻike loiloi, 60 mau pūpū o HPLC, 20 mau hoʻonohonoho o nā chromatographs hau, LCMS, ELSD, ultraviolet a me nā kikoʻī ākea ʻike, nā mea hana manuahi me nā mea hana loea. Ua hala ia ʻo ISO14001, ISO9000 a me DMF e hōʻoia ana ma o nā hōʻuluʻulu ʻana a me ka loaʻa ʻana, a loaʻa iā ia kahi ʻina hoʻokele piha.

Hoʻohui kā mākou hui i kekahi o nā loea o nā poʻe loea he mea noiʻi o ka honua holoʻokoʻa, a loaʻa iā ia nā ikaika piha o nā loiloi lab, hoʻokolohua hoʻoliʻi a me nā hana hana ʻenehana.
Aia nā kauka he 11 a ma mua o 46 mau haku, nā ʻepekema, a me nā mea hana ʻenehana i kā mākou hui.ʻO ka papa hana hoʻoliʻi API e uhi ana i kahi wahi o luna o 40 mu.The GMP pharmaceutical plant e uhi ana i kahi o ka nui o 160mu a he kekelē o kēia puʻenehana, ʻĀpana hoʻokele a me nā hale ʻike. , he hale pule, kahi wahi haki, a oi.

"ʻO CMOAPI ka ISO 9001: 2008 ua hōʻoia ʻia a me kāna mau hana ʻoihana āpau e hoʻokō pono ana i nā kūlana hoʻokele o ka honua."

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DMF

Ua hōʻoia ʻia ʻo DMF

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9001

ISO

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14001

ISO

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ʻO nā kānakaʻepekema