Upcoming public courses in the next 90 days.

New! AI in Management Systems: Implementing ISO/IEC 42001:2023 in the Life Sciences

New! QMS Training for Medical Devices: ISO 13485:2016 and FDA QMSR

ISO 13485:2016 Lead Auditor Training

New! Transition from the FDA’s Quality System Regulation (QSR) to the Quality Management System Regulation (QMSR) - DaySmart Series

ISO 14971 Medical Device Risk Management and Analysis Training

Medical Device CAPA and Root Cause Investigation Training

Medical Device Design Control Training: FDA, ISO 13485 & MDSAP

EU MDR Training for Auditors (Medical Device Regulation 2017/745)

Implementation Training for the EU MDR (Medical Device Regulation 2017/745)

ISO 13485:2016 Internal Auditor Training

Internal Auditing to MDSAP: Concepts and Practices in Aligning the Internal Audit Program

Medical Device Complaint Handling, Event Reporting, and Recall Management Training

EU Clinical Evaluation Report (CER) Training for Medical Devices

Medical Device Supplier Quality Management Training

Medical Device Production and QMS Software Validation Training

ISO 9001:2015 Internal Auditor Training

Implementation Training for the EU IVDR (In Vitro Diagnostic Regulation 2017/746)

FDA and EU Medical Device Software Regulations and Standards Training

Medical Device Single Audit Program (MDSAP) Training

FDA Part 11 Compliance and Medical Device Data Integrity Training

US FDA and EU Regulatory Requirements Training for Combination Products

New! Good Laboratory Practices (GLP) Auditor Training

New! Investigations Into Deviations and Out-of-Specification (OOS) Test Results in Pharmaceutical Manufacturing

Upcoming public courses in the next 90 days.

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New! AI in Management Systems: Implementing ISO/IEC 42001:2023 in the Life Sciences

New! AI in Management Systems: Implementing ISO/IEC 42001:2023 in the Life Sciences

New! QMS Training for Medical Devices: ISO 13485:2016 and FDA QMSR

New! QMS Training for Medical Devices: ISO 13485:2016 and FDA QMSR

New! Transition from the FDA’s Quality System Regulation (QSR) to the Quality Management System Regulation (QMSR) - DaySmart Series

New! Transition from the FDA’s Quality System Regulation (QSR) to the Quality Management System Regulation (QMSR) - DaySmart Series

New! Good Laboratory Practices (GLP) Auditor Training

New! Good Laboratory Practices (GLP) Auditor Training

New! Investigations Into Deviations and Out-of-Specification (OOS) Test Results in Pharmaceutical Manufacturing

New! Investigations Into Deviations and Out-of-Specification (OOS) Test Results in Pharmaceutical Manufacturing