Controversy & Confusion: What Does Annex Z of EN/ISO 14971: 2012 Mean & How Can We Practically Implement It?




Pharmaceuticals & Biotechnology | Pharma & Biotech Resources show

Summary: Chuck 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 risk management under the European Medical Device Directives, how the expectations for risk