Courses #FDA - Eventura.site

Validation of Systems Using Artificial Intelligence (AI), Machine Learning (ML), Blockchain and ChatGPT for FDA Compliance

Change Control Management (CCM)

AI in Drug Discovery: Aligning with FDA's Latest Risk-Based Framework

Risk Management for AI in Medical Devices: Insights from FDA’s Life Cycle Management Draft Guidance

Reverse Engineering Medical Device Design Outputs

Good Documentation Practices (GDocP)

Post-Market Surveillance and Real-World Evidence

The DHF, Technical Documentation - Similarities, Differences and the Future

Live In-Person Seminar on Implementing CSA for GxP Systems - Transition, Documentation, and Post-Transition Challenges and Opportunities - Richmond, VA

Implementing CSA for GxP Systems - Transition, Documentation, and Post-Transition Challenges and Opportunities

FDA's Total Product Life Cycle Approach to In Vitro Diagnostic Products (IVD's)

Reclassification of Software Automated Medical Devices

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