Die Seminar-Inhalte
• Forderungen der EU-Richtlinien für Medizinprodukte und Qualitätsmanagement-Normen zum Risikomanagement
• Inhalte & Neuerungen im Risikomanagement nach ISO 14971:2012
• Durchführung und Dokumentation des Risikomanagements mit der en.co.tec Toolbox:
- Risikomanagementplan
- Risikomanagementakte
- Risikomanagementbericht
• Übungsbeispiel Risikomanagement-Akte
Teilnehmer
• QM- und Sicherheitsbeauftragte
• Produktmanager, Entwickler
• Mitarbeiter Regulatory Affairs
• Interessierte aus anderen Bereichen
Information on participating / attending:
Date:
03/07/2017 09:30 - 03/07/2017 17:00
Event venue:
Forum MedTech Pharma e.V., Rathenauplatz 2
90489 Nürnberg
Bayern
Germany
Target group:
Business and commerce, Scientists and scholars
Email address:
Relevance:
transregional, national
Subject areas:
Economics / business administration, Medicine, Nutrition / healthcare / nursing
Types of events:
Seminar / workshop / discussion
Entry:
01/02/2017
Sender/author:
Sandra Karakaya
Department:
Pressestelle
Event is free:
no
Language of the text:
German
URL of this event: http://idw-online.de/en/event56327
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