How to Implement and Maintain a Modern CAPA System while Avoiding Common Pitfalls
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Refuse to Accept & Additional Information Request: Avoiding Problems with Medical Device Submissions
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Preparing Your Technical Documentation under MDR: Proven Tips & Techniques
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Beyond Design Controls 101: Following the Regulation vs. Understanding its Intent
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Avoid Death by CAPA: The Modern Approach to Quality Event Management
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How to Apply Risk Management Throughout the Product Lifecycle of Your Medical Device
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How do you determine the root cause for a CAPA?
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How to Implement and Maintain a Modern CAPA System While Avoiding the Common Pitfalls
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