LENTILLES

- To ensure that the conformity of MD is properly verified, in accordance with the QMS before the release of a MD - Release of MD - To ensure that the technical documentation and the EU DoC are established and kept up to date - To ensure that the manufacturer applies and updates a PMS system in compliance with Regulation 2017/745 - Notifications to authorities - In the case of a MD subject to investigation, the statement that the MD complies with the GSPR is issued - Recall director