1. This training course is intended for both manufacturers and distributors of medical devices and will look at the current general obligations under Belgian law to place a medical device on the market.

    Both local pre-marketing (such as registration) and post-marketing (such as vigilance) obligations will be addressed.

    The presenters will also discuss the Belgian implementation of the Medical Devices Regulation (EU) 2017/745 (MDR), mainly focusing on the recent Belgian law of 22 December 2020 on medical devices (setting out the MDR implementation specifics for Belgium) and accompanying decrees which entered into force on 26 May 2021. 

    Prijs:beMedTech lid: 400,00 € (excl. BTW)
    Niet-lid beMedTech: 600,00 € (excl. BTW)
    Programma + sprekers:20211022 - Legislation of medical devices .pdf