| QS1019 | The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements | Arlington | VA | Oct 28, 2019 |
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| RM1119 | Integrating Risk Management into the Product Life Cycle | Arlington | VA | Nov 13, 2019 |
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| QS1219 | The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements | Arlington | VA | Dec 09, 2019 |
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| DC1219 | Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485 | Arlington | VA | Dec 10, 2019 |
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| DC0120 | Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485 | Arlington | VA | Jan 28, 2020 |
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| QS0220 | The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements | Arlington | VA | Feb 10, 2020 |
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| RM0320 | Integrating Risk Management into the Product Life Cycle | Arlington | VA | Mar 10, 2020 |
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| DC0320 | Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485 | Arlington | VA | Mar 24, 2020 |
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| PV0420 | Process Validation for Medical Devices: Requirements and Standards | Arlington | VA | Apr 14, 2020 |
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| QS0420 | The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements | Arlington | VA | Apr 27, 2020 |
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| CP0620 | Corrective and Preventive Action Requirements and Industry Practice | Arlington | VA | Jun 02, 2020 |
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