| QS0619 | The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements-June 2019 | Arlington | VA | Jun 24, 2019 |
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| RM0819 | Integrating Risk Management into the Product Life Cycle - July 2019 | Arlington | VA | Jul 30, 2019 |
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| QSIH090919 | AAMI/CQT Solutions The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements- September 2019 Ireland | Dublin | | Sep 09, 2019 |
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| QS0919 | The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements-September 2019 | Arlington | VA | Sep 16, 2019 |
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| DC0919 | Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485 - September 2019 | Arlington | VA | Sep 24, 2019 |
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| PV1019 | Process Validation for Medical Devices: Requirements and Standards - October 2019 | Arlington | VA | Oct 08, 2019 |
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| QS1019 | The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements- October 2019 | Arlington | VA | Oct 28, 2019 |
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| RM1119 | Integrating Risk Management into the Product Life Cycle - November 2019 | 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- December 2019 | Arlington | VA | Dec 09, 2019 |
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| DC1219 | Design Control Requirements • Integrating the Quality System Regulation and ANSI/AAMI/ISO 13485 - December 2019 | Arlington | VA | Dec 10, 2019 |
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