Harmonization of Software Requirements through Standards
Add bookmark
Harmonization of Software Requirements through Standards
Add bookmark
Rainer Voelksen, Vice-President for International Regulatory Affairs at Edwards Lifesciences, joins Pharma IQ to discuss why standards should have internationally compatible software requirements. He also touches upon the European QM approach, the GHTF project and the International Medical Device Regulator Forum in the interview.
[inlinead]
Rainer Voelksen will be among the speakers at the forthcoming conference: Software Design for Medical Devices Europe 2013, taking place 29 January - 01 February, 2013 - Munich, Germany. Please visit www.sdmdeurope.com for details, Contact us on 0800 652 2363 or +44 (0) 20 7368 9300 or email enquire@iqpc.co.uk now!
Tags:
Rainer Voelksen
Edwards Lifesciences
International Medical Device Regulator Forum
software requirements
software design medical devices
Software design
European QM approach
