3000031 Medical Device Software per IEC 62304
1000916 Speaker Data Sheet
6002220 Scheduled Sessions
3000021 Scrutinizing Test Method Validation (TMV) to Verify the Performance of a Medical Device
3000026 Risk Management for Medical Devices per ISO 14971
3000027 Through the Eyes of an Auditor
3000028 Chipping Away at Constraints
3000029 Process Validation Requirements & Compliance Strategies
3000030 Effective Design of Experiments (DOE) Strategies
3000032 Risk-based Design Control - The New Paradigm for Medical Device Design
3000033 Managing The Audit Function In A Global Company
3000040 FDA Regulation of Artificial Intelligence & Machine Learning
3000041 How to Conduct a Human Factors Usability Validation
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3000031 Medical Device Software per IEC 62304