WS_2.1

WS 2.1 - MDR Workshop

Anforderungen der neuen Medical Device Regulation an medizinische Software
Replay recorded session (participants only)

Moderator
	Martin Mayer, MSc. Technologieexperte Medtech & Digital Health, LISA Vienna
	Durch die Covid-19 Pandemie wurde das Inkrafttreten der Medical Device Regulation auf den 26. Mai 2021 verschoben. Auf die Unternehmen kommen zahlreiche Änderungen und Herausforderungen zu. In dieser Session erfahren Sie die wichtigsten Neuerungen und bekommen einen praxisnahen Einblick in die Zulassung nach MDR.

Speakers
	Dipl.-Ing. Martin Schmid Geschäftsführer & Senior-Consultant, en.co.tec	Download presentation: Download

	Nilaykumar Patel, MSc. contextflow
	DI Magdalena Kedwani contextflow	Download presentation: Download

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WS_2.1

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