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How Much Data is “Sufficient”? Navigating Clinical Evidence Requirements Under the MDR and IVDR
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Emerging Trends in Global Regulations: Insights Into More Efficient Regulatory Writing Practices
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Considerations for Companion Diagnostics: Lessons Learned and Key Takeaways from DIA 2024
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Devices in Focus: How to Save Time & Money with Real World Evidence
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Practical Strategies to Successfully Navigate Key IVDR Regulations Applicable to SaMD Devices
56:02