Software design
20th Software Design for Medical Devices Summit in Boston Chaired by Phani Bidarahalli, Wipro
October 27 by Pharma IQ(San Francisco, CA.) IQPC’s 20th Software Design for Medical Devices Summit is pleased to announce that Mr. Phani Bidarahalli, GM & Head of Healthcare Engineering at Wipro is chairing the...
Software Innovation: Heart Attack Intelligence
October 12 by Pharmaceuticals & Biotechnology EditorIf a patient is rushed into theatre with a heart attack, firstly a catheter will be placed in the arteries of the patient’s heart. Then physicians or the cardiologists can usually start with t...
Fire Your Medical Device Questions For The MHRA This Way
September 30 by Pharma IQ Surveys[surveycode]
Software Design for Medical Devices 2015 Research
September 07 by Pharma IQ SurveysPharma IQ invites you to take part in a short survey, on the topic of Software Design for Medical Devices. The survey consists of 12 questions and will take less than 5 minutes to complete. As...
Five Expert Perspectives on Software Design for Medical Devices
March 12 by Pharmaceuticals & Biotechnology EditorTo preview the interactive discussion that will take place at the 19th Software Design for Medical Device Summit taking place this May 11th & 12th in San Francisco,, we wanted to share the insig...
Choosing The Right System Software For Medical Devices
February 03 by Pharmaceuticals & Biotechnology EditorFinding the right software for the design of medical devices is critical, as there is little room for error. Developers have many choices to make, from whether to use a “roll-your-own” s...
Understanding How to Engage Clinicians - An Insider’s Guide
April 29 by Pharmaceuticals & Biotechnology EditorWe’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...
Pressures of Software for Medical Devices
December 02 by Pharma IQIn the medical device industry, the issue of software design is an important one. It can not only improve homogeneity and streamline processes, allowing for increases in safety and production, bu...
Risk Management for Software Design in Medical Devices from IEC 62304 and ISO 14971 Perspectives
March 31 by Pharma IQ NewsNEW YORK, NY AND SAN DIEGO, CA – (BUSINESSWIRE) –Software quality for safety-critical medical devices has been at the centre of discussion for industry experts and especially the FDA. In...