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FDAnews New Workshop -- Software and Cybersecurity Risk Management for Medical Devices: Understanding the FDA's Position and Best Practices for Compliance, April 14-15, 2015 | ||
By: PR Newswire Association LLC. - 27 Feb 2015 | Back to overview list |
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FALLS CHURCH, Va., Feb. 27, 2015 /PRNewswire-iReach/ -- Software and Cybersecurity Risk Management for Medical Devices: Photo - http://photos.prnewswire.com/prnh/20150226/178223 This workshop — chaired by internationally renowned expert Fubin Wu — has been specifically designed to provide attendees with industry best practices to achieve compliance and effectively assure medical device software safety. In fact, it's a once-in-a-lifetime opportunity to learn how the FDA expects manufacturers to manage the risks of medical devices that contain software. In two days of intensive sessions, attendees will be brought up to date on the FDA's latest research on medical device software best practices, software risk management related standards and guidances and key success factors for effective software risk management. Plus, in a special bonus, attendees will find out more about assurance levels and what it will take to convince regulators in one of seven invaluable case studies, always a popular and valuable way to learn. Spread throughout the course will be lessons in applying these key software risk management related standards and guidances to the software development processes:
During each teaching session, Mr. Wu will share techniques and best practices on how to:
Special Take-Home Resource Kit: Who Will Benefit:
Meet the Instructor: Conference Details: Tuition: $1,797 Easy Ways to Register: About FDAnews: Media Contact: Michelle Butler, FDAnews, 703-538-7665, mbutler@fdanews.com News distributed by PR Newswire iReach: https://ireach.prnewswire.com
SOURCE FDAnews |
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Copyright 2015 PR Newswire Association LLC. | Back to overview list |