About
The In vitro diagnostics Regulation (EU) 2017/746 entered into force on May 26th 2017 as the replacement of Directive on In vitro diagnostic medical devices (98/79/EC).
This regulation will be fully applicable from May 26th 2022, with the aim to increase safety and efficiency in the EU medical device market.
This training is developed to help in vitro diagnostic medical devices manufacturers understand which is the impact of the new In vitro diagnostic regulation (IVDR), the most relevant changes against the directive and how it will impact to either medical devices already in the market and new medical devices.