This course has been designed to learn design control, design verification, design validation, Design History File (DHF), use concepts and implement, learn about planning (inputs/outputs), and risk analysis to ensure your organization\'s devices meet intended uses / user needs and specified requirements. Learn about control of design changes and their results as well as transfer (design to product manufacturing).
Participants will understand FDA, design control, the life cycle of the product, the Design History File (DHF) and Device Master Record (DMR).
Who Should Attend?
The target audience for this course consists of managers and professionals work in quality (QA/QC), compliance / regulatory affairs, manufacturing (operations), or engineering (design).
Medical Device background, those in quality / regulatory affairs responsible for design control.
Please Note: Price includes materials, and certificate of attendance.
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Quality & Productivity Solutions, Inc. is an international firm dedicated to providing practical and effective consulting and training to achieve client objectives. Whether it’s improvement in process, product, service, or overall performance, exceptional results are our business. We partner with...
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