This course will introduce all necessary steps to design, implement and test critical medical devices in a regulatory compliant environment. This course will additionally address the software risk management and the resulting interfaces to device level risk management.
2-day In-person Seminar on 鈥淎pplying ISO14971:2012 and IEC62304 - A Guide to Practical Risk Management鈥� in London UK
27 - 28 October 2014, London, United Kingdom
Introduction
Venue
London, UK
London, UK, WILL BE ANNOUNCED SOON, London, United Kingdom
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Organised by
GlobalCompliancePanel
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