Lean Six Sigma Training and Certification

In 1998, GE hired Oriel STAT A MATRIX to develop and implement their Green Belt, Black Belt, and Master Black Belt programs. Since then, we’ve been an industry leader in Lean and Six Sigma training.
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Medical Device RA/QA

New! Inspection and Audit Readiness Training for Medical Device Manufacturers Topic Medical Device QMS Auditing	Public View Dates Private Contact Us
New! QMS Training for Medical Devices: ISO 13485:2016 and FDA QMSR Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
ISO 13485 Lead Auditor Training Course Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
New! Transition from the FDA’s Quality System Regulation (QSR) to the Quality Management System Regulation (QMSR) - DaySmart Series Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
ISO 14971 Medical Device Risk Management and Analysis Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Medical Device QMS Overview Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Medical Device CAPA and Root Cause Investigation Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Medical Device Design Control Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
EU MDR Auditor Training Course for Europe’s Medical Device Regulation (2017/745) Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
EU MDR Training for the European Medical Device Regulation (2017/745) Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
ISO 13485 Internal Auditor Training Class Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Medical Device Single Audit Program (MDSAP) Internal Auditor Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Medical Device Complaint Handling, Event Reporting, and Recall Management Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
EU MDR CER (Clinical Evaluation Report) Training for Medical Devices Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Medical Device Software Development Life Cycle (SDLC) and IEC 62304 Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Medical Device Supplier and Subcontractor Quality Management Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Performance-Based Auditing for Medical Devices - A Tool for FDA’s Case for Quality Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Understanding FDA’s Medical Device Quality System Regulation Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
New! Inspection and Audit Readiness Training for Medical Device Manufacturers Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Medical Device Process Validation Training Course: FDA and ISO 13485 Requirements Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Medical Device Production and QMS Software Validation Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
ISO 13485 Overview Training for Medical Device and IVD Manufacturers Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
ISO 9001 Internal Auditor Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Combination Device Supplier Management Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
EU IVDR Auditor Training Class (2017/746) Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Medical Device Cybersecurity Risk Management, Regulations and Standards Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
EU In Vitro Diagnostic Regulation Overview Training (IVDR 2017/746) Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Medical Device Postmarket Surveillance (PMS) Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
FDA and EU Medical Device Software Regulations and Standards Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
FDA and EU Medical Device Labeling Requirements Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Inspection and Audit Readiness Training for Medical Device Manufacturers Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Inspection and Audit Readiness Training for Medical Device Manufacturers Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
FDA and EU Medical Device Classification and Regulatory Pathway Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
ISO 14971 and Risk Management Training for Combination Drug-Device-Biologic Products Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Medical Device Single Audit Program (MDSAP) Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
FDA 21 CFR Part 11 Training: Pharmaceutical Data Integrity, ALCOA+, and Electronic Records Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
FDA Part 11 Compliance and Medical Device Data Integrity Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
ISO 9001:2015 Lead Auditor Training Course Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Lean Six Sigma Champion Training Course Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Lean Six Sigma Champion Training Course Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
US FDA and EU Regulatory Requirements Training for Combination Products Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Design Control Training for Drug-Device and Other Combination Products Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Medical Device SOP Writing and Process Mapping Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
FDA GMP Inspection and For Cause Audit Training for Combination Products Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Lean Six Sigma Black Belt Certification Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Lean Six Sigma Black Belt Certification Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Lean Six Sigma Master Black Belt Certification Training Course Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Lean Six Sigma Master Black Belt Certification Training Course Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Training on How to Conduct a Remote Medical Device QMS Audit Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Root Cause Analysis for Combination Products and Drug Delivery Systems Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Root Cause Analysis for Combination Products and Drug Delivery Systems Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Medical Device Human Factors Usability and IEC 62366 Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us
Drug Delivery System Human Factors and Usability Requirements Training Topic Medical Device RA/QA Training	Public View Dates Private Contact Us

Pharmaceutical RA/QA

New! FDA GMP Inspection and For Cause Audit Training for Combination Products Topic Regulatory Compliance for Pharmaceuticals	Public View Dates Private Contact Us
New! Root Cause Analysis for Combination Products and Drug Delivery Systems Topic Regulatory Compliance for Pharmaceuticals	Public View Dates Private Contact Us
New! Investigations Into Deviations and Out-of-Specification (OOS) Test Results in Pharmaceutical Manufacturing Topic Regulatory Compliance for Pharmaceuticals	Public View Dates Private Contact Us
Pharmaceutical Process Validation Training Topic Regulatory Compliance for Pharmaceuticals	Public View Dates Private Contact Us
Drug Delivery System Human Factors and Usability Requirements Training Topic Regulatory Compliance for Pharmaceuticals	Public View Dates Private Contact Us

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Medical Device RA/QA

New! Inspection and Audit Readiness Training for Medical Device Manufacturers

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

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

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