IEC 60601-1 3rd Edition, Part 4 – Risk Management Posted by Bob Duffy on May 27, 2019 in Design, Device Tips Design, IEC 60601-1 3rd Edition, Risk Management View
IEC 60601 3rd Edition – The 3 Collaterals Posted by Bob Duffy on May 25, 2018 in Design, Device Tips Collateral, Design, Development, Risk Management, Software, Usability, Validation, Verification View
Complete Electronic Hardware Design Package Posted by Bob Duffy on May 19, 2015 in Design, Device Tips Electronic Hardware, Electronic Hardware Design Package, Hardware Design View
Software Development Management, Part 2, Software Requirements Posted by Bob Duffy on March 18, 2014 in Design, Device Tips Compound Software Requirements, Software Requirements, Software Requirements and Specifications View
Software Development Management, Part 1, Overview Posted by Bob Duffy on November 22, 2013 in Design, Device Tips Medical Device Development, Software Architecture, Software Design, Software Design Transfer, Software Development, Software Development Plan, Software Development Process, Software Requirements and Specifications, Software Validation, Software Verification View
3 C’s of Specifications Posted by Bob Duffy on September 10, 2013 in Design, Device Tips Design Input, FDA, Medical Devices, QSR, Specifications View
