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Eventura.site
Eventura World
Courses
Blogs
Courses #Medical Device
Bottlenecks to Flow: Optimizing Design Controls and Validation in Medical Device QMS
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AI in Drug Discovery: Aligning with FDA's Latest Risk-Based Framework
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Risk Management for AI in Medical Devices: Insights from FDA’s Life Cycle Management Draft Guidance
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Reverse Engineering Medical Device Design Outputs
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FDA Inspections and Audit Readiness Course
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Scrutinizing Test Method Validation (TMV) to Verify the Performance of a Medical Device
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FDA's Total Product Life Cycle Approach to In Vitro Diagnostic Products (IVD's)
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Reclassification of Software Automated Medical Devices
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FDA's Total Product Life Cycle Approach to In Vitro Diagnostic Products (IVD's) - Copy
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Design Control For Medical Devices And Combination Products
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Data Integrity – In Compliance with CSA, 21 CFR Part 11, SaaS/Cloud, EU GDPR
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STATISTICAL PROCESS CONTROL (SPC) AND CONTROL CHARTS - IN ACCORDANCE WITH LATEST FDA EXPECTATIONS
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