Isu tinofara kuzivisa kugamuchira kweMedical Device Single Audit Program certification (#MDSAP). MDSAP ichatsigira kubvumidzwa kwekutengeserana kwezvigadzirwa zvedu munyika shanu, kusanganisira Australia, Brazil, Canada, Japan neUS.
MDSAP inobvumira kuitwa kwekamwe ongororo yekutarisa kwemhando yegadziriso yemugadziri wemidziyo yekurapa kugutsa zvinodikanwa zvematunhu akawanda ekutonga kana zviremera zvinogonesa kutarisisa kwakakodzera kwemaitiro evagadziri vezvishandiso zvekurapa uku uchideredza mutoro wekutonga paindasitiri. Chirongwa ichi parizvino chinomiririra Therapeutic Goods Administration yeAustralia, Agência Nacional de Vigilância Sanitária yekuBrazil, Health Canada, Ministry of Health, Labor and Welfare uye Pharmaceutical and Medical Devices Agency, uye US Food and Drug Administration's Center for Devices and Radiological Health.
Nguva yekutumira: Kubvumbi-13-2023