Harmonization of Software Requirements through StandardsHosted By : Helen Winsor
December 3, 2012
Rainer Voelksen | Edwards Lifesciences | International Medical Device Regulator Forum | software requirements | software design medical devices | software design | European QM approach
About this Podcast...
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.
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 email@example.com now!
to get access to this White Paper
comments powered by Disqus
DoubleTree by Hilton Hotel - Victoria, London, United Kingdom
April 28- 30, 2014
17th Software Design for Medial Devices
San Francisco, CA
May 19- 19, 2014
Medical Device UDIs & Traceability Forum
May 20- 22, 2014
E-notebooks: 2014 and Beyond
October 16, 2013
Drive Successful Commercial Product Launches through Effective Key Packaging
February 7, 2013