Verification and Validation – what is their contribution to medical device software development?
About this Podcast...
Klaus Moritzen, Process Manager for Verification and Validation at Siemens Healthcare, joins Pharma IQ to discuss the contribution of Verification and Validation to medical device software development.He also touches the dichotomy between regulatory compliance and value creation.
Have Your Say
Rate this feature and give us your feedback in the comments section below
Klaus Moritzen 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 http://www.sdmdeurope.com/ for details, Contact us on 0800 652 2363 or +44 (0) 20 7368 9300 or email email@example.com now!
comments powered by Disqus
RBC’s Epigenetics Toolbox: Enabling Epigenetic Research and Drug Discovery
November 20, 2014
5th Annual Pharmacovigilance Asia Summit
Grand Copthorne Waterfront Hotel, Singapore
November 25- 27, 2014
Cell Based Assays
December 3- 4, 2014
Product Inspection in the Packaging Industry - Are You Ready?
September 24, 2014
E-notebooks: 2014 and Beyond
October 16, 2013