PQMS Academy Course Catalog
PQMS Academy
Quality, Regulatory, and Management Training
Expert-led training to build skills, drive compliance, and improve performance across your organization.
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Medical Devices QMS
Lead Auditor and Internal Auditor training for medical device quality management systems.
- 4 days Lead Auditor Training
- 3 days Internal Auditor Training
Quality Management
Auditor training focused on quality management system requirements and practical implementation.
- 4 days Lead Auditor Training
- 3 days Internal Auditor Training
Medical Device Single Audit Program
Training on the MDSAP audit approach for medical device regulatory quality systems.
- 4 days Lead Auditor Training
- 3 days Internal Auditor Training
Aerospace QMS
Auditor training for aerospace quality management system requirements and practices.
- 4 days Lead Auditor Training
- 3 days Internal Auditor Training
Automotive QMS
Auditor training for automotive quality management system requirements.
- 4 days Lead Auditor Training
- 3 days Internal Auditor Training
Medical Device Risk Management
Risk management training for medical devices using ISO 14971 principles and expectations.
- 2 days Medical Device Risk Management
Workplace Organization
Training in Sort, Set in Order, Shine, Standardize, Sustain, and Safety methodology.
- 1 day 6S methodology
Production Approval & Quality Planning
Training on Production Part Approval Process and Advanced Product Quality Planning.
- 3 days Plan, Validate, Document, Approve
Eight Disciplines Problem Solving
Structured problem-solving from team formation through root cause, corrective action, prevention, and closure.
- 3 days Eight Disciplines
Six Sigma Black Belt
Training focused on Define, Measure, Analyze, Improve, and Control methodology.
- 5 days Six Sigma Black Belt
Green Belt Training
Lean Six Sigma Green Belt training for process improvement and performance excellence.
- 5 days Data-driven Process Improvement
European Medical Device Regulation
Training on EU MDR 2017/745 requirements for medical device quality and regulatory compliance.
- 2 days Medical Device Regulation