In Vitro Medical Devices Regulation
April 2017 on in vitro diagnostic medical devices and repealing directive . Products that comply with the standard . The ivdr is the new regulatory basis for placing on the market, making available and putting into service in vitro diagnostic medical devices on the european . (1) in addition to the functions conferred on the authority by regulation 3 of the european union (medical devices and in vitro diagnostic . Who global model regulatory framework for medical devices including in vitro diagnostic medical devices. Overview from health.ec.europa.eu In accordance with the regulation of the minister of health. The in vitro diagnostic medical devices regulation (eu) 2017/746 (ivdr) establishes a new regulatory framework for in vitro diagnostic medical . 189/2000 of 12 th august, transposing the directive 98/79/ce, an . The ivdr is the new regulatory basis for placing on the market, m