Am Montag, 14. November 2016, spricht ab 16.30 Dr. Bassil Akra von der TÜV Süd Product Service GmbH über die „Änderungen der regulatorischen Anforderungen in Europa im Zuge der Medical Device Regulation (MDR) und der In-Vitro-Diagnostika-Regulation (IVDR)“. MDR und IVDR stehen kurz vor ihrer Ratifizierung. Auf die Hersteller kommen damit einschneidende Änderungen bei klinischen Bewertungen und klinischen Studien zu. Auch für Vigilanz und Marktüberwachung gelten neue Regeln, ebenso für die Technische Dokumentation.
Information on participating / attending:
Für Besucher der MEDICA kostenfrei.
Date:
11/14/2016 16:30 - 11/14/2016 17:00
Event venue:
MEDICA
Messe Düsseldorf
Halle 15/A56
40474 Düsseldorf
Berlin
Germany
Target group:
Business and commerce, Scientists and scholars
Email address:
Relevance:
transregional, national
Subject areas:
Economics / business administration, Medicine
Types of events:
(Student) information event / Fair, Presentation / colloquium / lecture
Entry:
11/02/2016
Sender/author:
Jana Ehrhardt-Joswig
Department:
Redaktion/Öffentlichkeitsarbeit
Event is free:
yes
Language of the text:
German
URL of this event: http://idw-online.de/en/event55891
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