Since 2021, the UK has been offi­cial­ly sep­a­rat­ed from the EU reg­u­la­to­ry sys­tem. How­ev­er, CE-marked med­ical devices and IVDs are still accept­ed in the UK and this accep­tance will remain valid until 2030.  Man­u­fac­tur­ers out­side the UK must appoint a UK Respon­si­ble Per­son (UKRP) to place or con­tin­ue plac­ing their devices on the UK mar­ket. Sim­i­lar­ly, British … Con­tin­ue read­ing UK Respon­si­ble Per­son (UKRP)