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Change Management and Risk Management: How Do We Connect the Dots and What Happens if We Don’t?

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Preparing Your Technical Documentation under MDR: Proven Tips & Techniques

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How to Implement and Maintain a Modern CAPA System while Avoiding Common Pitfalls

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Align Your Clinical Claims with the Clinical Investigation Performance and Safety Endpoints

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Bridging User Needs & Design Requirements

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How to Apply Risk Management Throughout the Product Lifecycle of Your Medical Device

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How to Avoid Common Problems with your Design, Risk, and Validation Documentation

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How to Prepare for and Manage Audits/Inspections across Global Markets