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FDA -
Medical -
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ISO -
Risk -
Auditing
Recorded Webinars
John E Lincoln | View Anytime | 90 Minutes
Risk Management for AI in Medical Devices: Insights from FDA's Lifecycle Management Draft Guidance
John E Lincoln | View Anytime | 3 Hours
3-Hour Virtual Seminar on Master Validation Plan - The Unwritten Requirements
John E Lincoln | View Anytime | 90 Minutes
Medical Device Change(s) and the 510(k)
John E Lincoln | View Anytime | 90 Minutes
The DHF, DMR, DHR, and the Technical Documentation File - The US FDA and EU MDR Requirements
Ginette Collazo | View Anytime | 90 Minutes
Decision Making and Human Error
Ginette Collazo | View Anytime | 90 Minutes
5S for Operators and Human Error Reduction
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