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2014 - "Human Factors Engineering"
Date2014-09-15
Deadline2014-09-15
VenueOnline, USA - United States 
Keywords
Websitehttps://compliance2go.com
Topics/Call fo Papers
DESCRIPTION
Usability Engineering, (Human Factors Engineering) is an essential part of a device development program. In fact, a major issue arises when a device works correctly, but is used incorrectly. This is called “use error” and can cause harm to a patient or user.
If you have not implemented a Usability Engineering program, your design control system is not adequate. You open yourself up to audits, inspections, and product liability issues. The program will help you ensure your devices are used correctly and that ISO 14971:2007 risk reduction using information for safety is effective.
Usability Engineering, (Human Factors Engineering) is an essential part of a device development program. In fact, a major issue arises when a device works correctly, but is used incorrectly. This is called “use error” and can cause harm to a patient or user.
If you have not implemented a Usability Engineering program, your design control system is not adequate. You open yourself up to audits, inspections, and product liability issues. The program will help you ensure your devices are used correctly and that ISO 14971:2007 risk reduction using information for safety is effective.
Other CFPs
- "FDA Regulations for Food, Drugs, Biologics, Cosmetics, and Medical Devices Including IVDs"
- "Patient Rights and the HIPAA Privacy Officer - Meeting Patient Desires and Avoiding Penalties"
- "FDA Recordkeeping Requirements"
- "The FDA Inspection: Preparation, Performance, and Follow-up"
- "FDA 510(k) Update: Trends, New Strategy, Submission and FDA Clearance"
Last modified: 2014-08-08 19:39:25