CRO & CDMO

Cov txheej txheem dav dav tau teeb tsa los muab cov kev pabcuam CRO thiab CDMO nrog cov kws tshaj lij R & D pab pawg los ntawm peb cov neeg koom tes.

Cov kev pabcuam CRO raug suav nrog cov txheej txheem kev txhim kho, kev npaj thiab ua tus yam ntxwv ntawm cov qauv hauv tsev, kev kawm impurity, kev sib cais thiab kev txheeb xyuas rau cov paub thiab tsis paub impurities, analytical method development & validation, stability study, DMF and regulatory support, etc.

Cov kev pabcuam CDMO muaj xws li peptide API synthesis thiab purification txheej txheem kev txhim kho, ua kom tiav daim ntawv loj hlob, siv cov qauv kev npaj thiab kev tsim nyog, impurity thiab cov khoom zoo kawm thiab tshuaj xyuas, GMP system ntsib EU thiab FDA tus qauv, thoob ntiaj teb thiab Suav kev tswj hwm thiab kev txhawb nqa ntawv, thiab lwm yam.