Umufatanyabikorwa wizewe

Conlight Medical ifite kandi uruganda rwa GMP rukora ibikoresho n'ibinyabutabire byakozwe muri vitro. Yatsinze icyemezo cya ISO 13485 na Medical Device Single Audit Program (MDSAP) cyatanzwe n'Ikigo cy'Uburezi cya British Standards InstitutionBSI kandi ifite ubushobozi bukomeye bwo gukoresha ibikoresho.

Kugeza ubu, hubatswe imirongo 8 y’ibikoresho byo gusuzuma indwara mu buryo bwa “in vitro” n’ibikoresho by’ubuvuzi, bifite ubushobozi bwo gukora miliyoni 15 ku mwaka n’umusaruro ungana na miliyari 5 z’amayuani ku mwaka. Muri icyo gihe, ifite patenti mpuzamahanga ya mbere ya PCT ku bikoresho byo gupima ubuzima mu Bushinwa kandi ifite ibikoresho byo gupima birenga 50 byemejwe n’Umuryango w’Ubumwe bw’u Burayi.