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beMedTech Academy & Events

30/11/2021

Advertising of medical devices (including use of social media)

Since advertising of medical devices is a topic on which there is little legislation at European level, there are significant differences between jurisdictions. We will focus on the general national (Belgian) legal and regulatory framework applicable to advertising, and more specifically the promotion of medical devices in Belgium. Special attention will also be paid to the hot topic of advertising through social media and the new EU requirements regarding claims. This presentation is primarily intended for those who advertise medical devices in Belgium/the EU
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01/02/2022

Legislation IVDR + impact new regulation

The In Vitro Diagnostic Medical Device Regulation (EU) 2017/746 (IVDR) is set to significantly reshape the way IVDs are being marketed in the EU and will significantly amend the applicable legal framework from 26 May 2022. This presentation will identify the changes brought by the IVDR and the obligations of economic operators as from 26 May 2022, both in the pre-marketing and post-marketing phases, with tips and tricks to ensure compliance during and after the transition period. This presentation is primarily intended for those manufacturing or distributing IVDs in the EU.
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Secteur en chiffres

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16,820
FTEs

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2.4 milliards
(hors exportation)

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37.74 %
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