The Cutting Edge of Medical Technology Content, Community & Collaboration
Time: May 26, 2016 at 9am to May 27, 2016 at 6pm
Location: WILL BE ANNOUNCED SOON
City/Town: Washington, DC
Website or Map: http://bit.ly/design-controls…
Event Type: conference
Organized By: NetZealous DBA as GlobalCompliancePanel
Latest Activity: Apr 21, 2016
Human Factors/Usability testing is now a requirement. Human Factors/Usability testing is good business and can be easily integrated into product design/development. Human Factors is at the essence of the UseFMEA and hence instrumental in being able to reduce the probability of risk, and even the severity of risk. The key to integrating Human Factors is to understand the activities involved throughout the product development cycle and the corresponding design controls. These activities will be covered with the opportunity to implement on a real world problem/device. In addition, the appropriate documentation and content will be covered so that a full picture of the integration can be understood. Differences between European and US standards will be covered as required.
Why should you attend?
Do you feel that Human Factors slows the time to market and increases costs of your products? Do you feel that Human Factors documentation is foreign and cumbersome? If you have answered �yes� to these two questions then you need to find out that the correct answer is quite the opposite.
Human Factors/Usability testing is now a requirement. Human Factors/Usability testing is good business and can be easily integrated into product design/development. Human Factors is at the essence of the UseFMEA and hence instrumental in being able to reduce the probability of risk, and even the severity of risk.
Who Will Benefit:
Virginia A. Lang
Principal and Founder, HirLan, Inc. and HirLan International SA
Virginia started in the medical research field as a Coordinator of Research at the Clinical Research Unit Kennedy Institute of Johns Hopkins Medical Center. She was responsible for the initiation, coordination, and management and/or analysis of research projects in the Clinical Research Unit.
Location: Washington, DC Date: May 26th & 27th, 2016 Time: 9:00 AM to 6:00 PM
Venue: WILL BE ANNOUNCED SOON
Price: $1,295.00 (Seminar for One Delegate)
Register now and save $200. (Early Bird)
Until April 20, Early Bird Price: 895.00 from April 21 to May 24, Regular Price: $1,095.00
NetZealous DBA as GlobalCompliancePanel
Registration Link - http://bit.ly/design-controls-risk-analysis