Post-Market Surveillance for Medical Devices & Combination Products
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How to Implement and Maintain a Modern CAPA System while Avoiding Common Pitfalls
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Post-market surveillance as a medical device requirement in the EU
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The Global Guide to Human Factors and Usability Engineering Regulations
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Software Validation Documentation for Medical Devices - FDA eSTAR
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20 Life-Changing Medical Inventions
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How to Apply Risk Management Throughout the Product Lifecycle of Your Medical Device
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Industry-Presented Webinar: The Female Athlete Triad & Sports Nutrition Strategies for Recovery
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