API CDMO service Bahlahisi ba Pharmaceutical API

Tšebeletso ea CDMO ea API, Taolo e Felletseng ea Ts'ebetso

Feme ea letsoho, taolo ea boleng bo fapaneng

1, Maemo, Tlhahiso e pepeneneng

Khampani ea Hande, ho tloha setsing sa lifofane ho ea ho tlhahiso e kholo, e kopana le litekanyetso tsa setifikeiti sa GMP, 'me ts'ebetso eohle e emetsoe.Litšila le taolo ea bohloeki li kopana le litekanyetso tsa USP/EP/CP ho netefatsa boleng bo tšepahalang ba sehlahisoa.

2、 Linaha tse ngata, sistimi ea taolo ea boleng

Khampani ea Hande e thehile sistimi ea netefatso ea boleng ho latela litlhoko tse tloaelehileng tsa mmaraka joalo ka US FDA system le European Union. E na le libaka tse 13 tsa taolo ea boleng, taolo e felletseng le ho lateloa, 'me e fihlela litlhoko tsa tlhahlobo le tlhahlobo ea lichelete.

3, Lintlha tse felletseng le tse nepahetseng tsa tlhahlobo

Khamphani ea Hande, e nang le kamore ea tlhahlobo ea QC e iketselitseng, moralo o hlakileng oa sistimi le lisebelisoa tse felletseng tsa tlhahlobo, e ka fana ka lintho tsa tlhahlobo tse koahelang melao ea linaha tse ngata ho latela litlhoko tsa bareki ho netefatsa bonnete ba lintlha tsa tlhahlobo le ho thusa lipatlisiso tsa bongaka le nts'etsopele.

Hande fektheri 

Hande Bio, Ka lilemo tse 30 tsa semelo sa litsebo tsa limela le li-API, ha re barekisi ba nang le tsebo feela empa hape re ikhethile ka ho thusa lik'hamphani tsa meriana, lik'hamphani tsa lisebelisoa tsa bongaka, Brands tsa Health & Beauty ho nts'etsapele lihlahisoa tsa bona tse ncha.

Sehlopha sa rona sa litsebi se nang le R&D, taolo ea boleng le sistimi ea tlhahiso se tla u fa ts'ebeletso e le 'ngoe e nang le metsoako e tsoang ho litlolo tsa tlhaho, liforomo leKAROLO/CDMO/Regulatory Registration Filing.Fana ka ts'ehetso e felletseng le e hlophisitsoeng bakeng sa katoloso ea 'maraka oa hau, ha ho hlokahala, o ka ikopanya le rona.