software design medical devices
Key steps to advance medical device information security and privacy
May 07 by Patrick Reichmann
Patrick Reichmann discusses how to address the key regulatory challenges in the medical device industry
Understanding How to Engage Clinicians - An Insider’s Guide
April 29 by Pharmaceuticals & Biotechnology Editor
We’re not all the same Much has been written and said about the need to involve clinicians in the technology process. Increasing efforts are being made to understand doctors, nurses and oth...
Edwards Lifesciences' Rainer Voelksen on Harmonisation of Software Requirements through Standards
December 05 by Helen WinsorRainer Voelksen, Vice-President for International Regulatory Affairs at Edwards Lifesciences, joins Pharma IQ to discuss why standards should have internationally compatible software requirements. H...
Harmonization of Software Requirements through Standards
December 03 by Helen WinsorRainer Voelksen, Vice-President for International Regulatory Affairs at Edwards Lifesciences, joins Pharma IQ to discuss why standards should have internationally compatible software requirements. H...
Controversy & Confusion: What Does Annex Z of EN/ISO 14971: 2012 Mean & How Can We Practically Implement It?
December 03 by Helen WinsorChuck Sidebottom, Director, Corporate Standards at Medtronic and Dave Osborn, Manager, International Standards at Philips, join Pharma IQ to discuss the current controversy over the application of ris...
