Program Highlights:
- Post-Market Clinical Follow-Up for Medical Software, Dr. Manuela Schwegler, Expert Scientific & Regulatory Affairs, i.DRAS GmbH, Planegg/Martinsried
- Developments in Risk Management: the new ISO 14971, Hans Wenner, Owner, Engineering Office Wenner, Rüsselsheim
- Challenges in Quality Management for Medical Software, Prof. Dr. Mark Hastenteufel
Owner, dr-hastenteufel.de, Heidelberg
- The Technical Documentation as central Element for Market Access, Isabella Lehner
Senior Manager Regulatory Affairs, Croma Pharma GmbH, Vienna (Austria)
- Cybersecurity in U.S. Healthcare, Axel Wirth, Distinguished Technical Architect, Symantec Corporation, Boston (USA)
Learn at Medical Software 2019
- which future regulatory requirements you will have to meet,
- how to deal efficiently with them, and
- what the brand-new digital platform VDE Medical Software offers to you!
We would be pleased if you forwarded this invitation to all your colleagues.
See you in Frankfurt,
Thorsten Prinz
Information on participating / attending:
Please note our special early bird deal: If you register on our new digital platform VDE Medical Software (meso.vde.com) and book your ticket until April 15, 2019, admittance is free and no fee will be charged. Registering or booking your ticket later, the regular fee of 290 EUR will apply.
Date:
05/15/2019 10:00 - 05/15/2019 16:30
Event venue:
Tagungszentrum
Haus am Dom
Domplatz 3
60311 Frankfurt/M.
Hessen
Germany
Target group:
all interested persons
Email address:
Relevance:
international
Subject areas:
Medicine
Types of events:
Conference / symposium / (annual) conference
Entry:
02/11/2019
Sender/author:
Dr. Thorsten Prinz
Department:
Kommunikation + Public Affairs
Event is free:
no
Language of the text:
English
URL of this event: http://idw-online.de/en/event62810
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