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Quality Management Systems (QMS) training transforms a standard from a manual on a shelf into a competitive advantage by ensuring every employee understands how their specific role impacts product safety and customer satisfaction. Beyond simple compliance, a well-trained workforce reduces costly waste, streamlines operations through standardized processes and builds the institutional discipline required to win and retain high-value contracts in regulated industries.

Whether you need to train your team or require hands-on support to close system gaps, our end-to-end training programs, coaching and audit services are designed to streamline your journey toward a robust Quality Management System.

ISO 9001:2015
ISO 9001:2015

We provide a comprehensive path to compliance through our ISO 9001:2015 overview and internal auditor training, complemented by expert technical assistance and professional internal auditing services to ensure you are fully prepared for certification.

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ISO 9001 Overview

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The ISO 9001 Overview training equips organizations with the knowledge, tools, and roadmap needed to build an effective Quality Management System and confidently prepare for ISO 9001 certification.

Participants will:

  • Understand the structure, intent and requirements of ISO 9001 and how they apply to their organization
  • Identify gaps between current practices and ISO 9001 requirements through a practical readiness assessment
  • Develop a clear, step-by-step roadmap to achieve certification, including documentation and process needs
  • Learn how to implement and maintain a compliant Quality Management System (QMS)
  • Topics covered:

  • Overview of ISO 9001 and the Quality Management System (QMS) framework
  • ISO 9001 clauses, requirements and documentation expectations
  • Process mapping, risk-based thinking and performance measurement
  • Internal audits, management review and continual improvement
  • Certification readiness, audit preparation and next steps to registration
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Coaching:

    Customized coaching is available

    Recommended For:

    Quality managers, operations leaders, process owners, and cross-functional team members who are responsible for implementing, managing or preparing their organization for ISO 9001 certification—and for any organization seeking to improve consistency, efficiency and customer satisfaction through a structured Quality Management System.

    Contact your Regional Manager to schedule.

    ISO 9001 Internal Auditor Training

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    The ISO 9001 Internal Auditor training prepares participants to plan, conduct, and report effective internal audits that strengthen their Quality Management System and ensure ongoing compliance with ISO 9001 requirements.

    Participants will:

  • Understand ISO 9001 requirements and how they apply during an internal audit.
    Learn how to plan, conduct and document effective internal audits.
  • Develop the skills to identify nonconformities, risks and improvement opportunities
  • Gain confidence in interviewing, evidence gathering and audit reporting
  • Topics covered:

  • ISO 9001 requirements and the role of internal audits in a Quality Management System
  • Audit planning, preparation and audit program management
  • Conducting audits: interviewing, evidence collection and objective evaluation
  • Reporting findings, corrective actions and continual improvement
  • Audit follow-up, root cause analysis and verification of corrective actions
  • Duration:

    14-16 Hours | 2 Days

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Recommended For:

    Quality professionals, supervisors, managers and cross-functional team members who are responsible for conducting or supporting internal audits, maintaining ISO 9001 compliance and driving continual improvement within their organization.

    Contact your Regional Manager to schedule.

    ISO 9001 Internal Auditor Upgrade Training

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    ISO 9001 Internal Auditor Upgrade training helps experienced auditors stay current with the latest standard, refresh their auditing skills and enhance their ability to drive compliance, and continual improvement within their organization.

    Participants will:

  • Understand the changes and updates in the latest ISO 9001 standard
  • Refresh internal auditing skills and techniques for effective audits
  • Learn how to apply new requirements during audit planning and execution
  • Enhance their ability to identify nonconformities and improvement opportunities
  • Maintain competence to support certification audits and continual improvement initiatives
  • Topics covered:

  • Key changes and updates in the latest ISO 9001 standard
  • Impact of new requirements on internal auditing practices
  • Updated audit planning, preparation and execution techniques
  • Identifying and documenting nonconformities and improvement opportunities
  • Best practices for audit reporting, follow-up and supporting continual improvement
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Recommended For:

    Experienced internal auditors who need to update their knowledge and skills to align with the current version of the ISO 9001:2015 standard. It focuses on understanding what has changed in the standard, how those changes impact audit criteria and how to adjust audit practices to ensure continued compliance and audit effectiveness.

    Contact your Regional Manager to schedule.

    On-Demand Self-Paced ISO 9001 Overview

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    ISO 9001:2015 Self-Paced Overview provides a deep dive into the standard’s structure and requirements, offering management and implementation teams the actionable insights needed to maintain an effective Quality Management System

    Participants will:

  • Decode Requirements: Master the structure and core requirements of ISO 9001:2015
  • Apply Quality Tools: Learn to implement risk-based thinking and the Plan-Do-Check-Act (PDCA) cycle
  • Identify Gaps: Evaluate your current system to determine the specific steps needed for compliance
  • Define Roles: Understand management’s responsibilities and the impact on documentation and records
  • Earn PDHs: Receive a certificate of completion and 5 Professional Development Hours
  • Topics covered:

  • ISO 9001:2015 Structure & Requirements: A deep dive into the standard’s framework and what each clause means for your business
  • Risk-Based Thinking & PDCA: How to apply the Plan-Do-Check-Act cycle and manage organizational risk effectively
  • Documentation & Records: Understanding the specific requirements for maintaining “documented information” and organizational knowledge
  • Implementation & Leadership: Strategic steps for a successful rollout and the critical roles top management must play
  • Duration:

    5 Hours

    Format:

    On Demand, online course

    Recommended For:

    Management, quality professionals, and implementation teams tasked with mastering and applying the ISO 9001:2015 standard.

    Contact your Regional Manager to schedule.

    ISO 9001 Technical Assistance

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    ISO 9001 Technical Assistance service provides expert guidance and hands-on support to help organizations implement, maintain and optimize their Quality Management System for certification success and operational excellence.

    Duration:

    16 – 20 Days

    Format:

    Customized on-site, in-person assistance

    Contact your Regional Manager to schedule.

    ISO 9001 Internal Audit Services

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    Let our experts handle your ISO 9001 internal audits, giving you an objective perspective on your processes while you focus on running the business.

    Duration:

    Varies

    Format:

    On-site, in-person audit service

    Contact your Regional Manager to schedule.

    AS9100 Aerospace
    AS9100 Aerospace

    AS9100 training, combining foundational Overview and Internal Auditor training with expert coaching, technical assistance and professional internal audit services, streamlines your path to aerospace certification. Whether you need to build internal expertise or require hands-on support to close system gaps, our end-to-end approach ensures your organization is fully prepared for the rigors of the aerospace industry.

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    AS9100 Overview

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    AS9100 Overview training is a foundational course designed to help your team navigate complex industry requirements before starting the certification process.

    Participants will:

  • Decode AS9100 Requirements: Gain a clear understanding of the aerospace-specific clauses and how they differ from standard quality systems
  • Master Risk & Safety: Learn to implement critical controls for operational risk, product safety and counterfeit parts prevention
  • Identify System Gaps: Develop the skills to evaluate your current processes against aerospace standards to ensure certification readiness
  • Align Internal Processes: Understand how to integrate AS9100 requirements into your daily workflow without compromising efficiency
  • Prepare for the Audit: Build the confidence and technical knowledge needed to navigate a successful third-party certification audit
  • Topics covered:

  • AS9100 Structure: Understanding the specific aerospace additions to the ISO 9001 framework
  • Risk & Product Safety: Navigating the requirements for operational risk management and aerospace safety
  • Supply Chain Integrity: Strategies for counterfeit parts prevention and enhanced supplier controls
  • Operational Controls: Mastering configuration management, traceability and product realization
  • Certification Roadmap: Preparing for gap analysis and the Stage 1 and 2 audit process
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Coaching:

    Customized coaching is available

    Recommended For:

    Aerospace leadership, quality managers and implementation teams preparing for AS9100 certification.

    Contact your Regional Manager to schedule.

    AS9100 Internal Auditor Training

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    AS9100 Internal Auditor training provides the practical tools needed to conduct thorough internal audits, ensuring your organization is confident and fully prepared for the road to certification.

    Participants will:

  • Master Auditing Techniques: Learn the professional principles and practices for conducting effective internal audits in the aerospace industry
  • Identify System Gaps: Develop the skills to spot non-conformities and system weaknesses against AS9100 requirements
  • Apply Aerospace Controls: Understand how to audit critical industry-specific areas, such as product safety and counterfeit parts prevention
  • Report Actionable Findings: Document and present audit results that drive continuous improvement
  • Drive Audit Readiness: Build the confidence to ensure your Quality Management System (QMS) is prepared for third-party certification
  • Topics covered:

  • Auditing Principles: Understanding the fundamentals of ISO 19011 and the requirements for an effective internal audit program
  • Aerospace-Specific Clauses: Deep-dive auditing techniques for product safety, risk management and counterfeit parts prevention
  • Audit Planning & Prep: How to develop checklists, define audit scopes and prepare for a process-based audit
  • Evidence Collection: Techniques for conducting interviews, sampling records and verifying compliance through observation
  • Reporting & Corrective Action: Mastering the art of writing clear non-conformity reports and evaluating the effectiveness of follow-up actions
  • Duration:

    14-16 Hours | 2 Days

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)
    * Visit our Courses for scheduled open enrollment sessions

    Recommended For:

    Quality professionals, engineers, and internal audit teams who need to develop the specialized skills required to evaluate and maintain an AS9100-compliant management system.

    Contact your Regional Manager to schedule.

    AS9100 Internal Auditor Training Upgrade

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    AS9100 Internal Auditor Training Upgrade provides experienced auditors with the targeted knowledge needed to evaluate aerospace-specific requirements, ensuring your organization is fully prepared for a successful pre-certification audit.

    Participants will:

  • Identify Aerospace Deltas: Master the specific requirements AS9100 adds to the ISO 9001 foundation
  • Audit High-Risk Areas: Develop the skills to evaluate complex aerospace controls like product safety and operational risk
  • Prevent Counterfeit Parts: Learn how to audit and verify robust systems for counterfeit parts prevention and detection
  • Audit Configuration Management: Understand how to verify traceability and technical documentation throughout the product lifecycle
  • Enhance Audit Depth: Transition from general quality auditing to high-level, process-based auditing, as required by the aerospace industry
  • Topics covered:

  • AS9100 “Delta” Requirements: Identifying the specific additions and enhancements that separate AS9100 from ISO 9001
  • Operational Risk & Safety: Auditing techniques for operational risk management and maintaining product safety throughout the lifecycle
  • Counterfeit Parts Prevention: Verifying the effectiveness of controls designed to prevent, detect and mitigate counterfeit parts
  • Configuration & Traceability: Evaluating systems for configuration management and the rigorous traceability required in aerospace
  • Human Factors & Ethics: Understanding how to audit the impact of human factors on quality and the importance of ethical behavior in the supply chain
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Recommended For:

    Experienced ISO 9001 internal auditors who need to bridge the gap and master the additional, specialized requirements unique to the AS9100 aerospace standard.

    Contact your Regional Manager to schedule.

    AS9100 Technical Assistance

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    AS9100 Technical Assistance provides hands-on, expert support to help you develop aerospace-compliant documentation, close system gaps, and implement critical controls like risk management and counterfeit parts prevention. This personalized service ensures your Quality Management System is fully optimized and audit-ready before your official third-party certification assessment.

    Duration:

    16-20 Days

    Format:

    Customized on-site, in-person assistance

    Contact your Regional Manager to schedule.

    AS9001 Internal Audit Services

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    Hiring our team to perform your AS9100 Internal Audit provides an objective, expert evaluation of your system, ensuring all aerospace-specific requirements are met without the bias or resource strain of using internal staff. By leveraging our deep industry knowledge, you receive a rigorous “dry run” that identifies critical gaps in areas such as product safety and risk management, significantly increasing your confidence and success rate in the official certification audit.

    Duration:

    Varies

    Format:

    On-site, in-person audit service

    Contact your Regional Manager to schedule.

    IATF 16949 Automotive
    IATF 16949 Automotive

    IATF 16949 automotive training provides a full spectrum of support, from foundational Overview and Internal Auditor training to personalized coaching and technical assistance designed to master the Core Tools (APQP, FMEA, SPC, MSA, PPAP). Whether you need to build in-house expertise or prefer our team to conduct your Internal Audit Services, we ensure your quality management system is optimized to reduce waste and meet the rigorous demands of global automotive OEMs.

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    IATF 16949 Overview

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    IATF 16949 training course equips automotive suppliers with the knowledge and tools needed to build a compliant quality management system and successfully prepare for certification.

    Participants will:

  • Understand the core requirements of IATF 16949 for automotive quality systems
  • Learn how to apply process-based and risk-based thinking
  • Identify gaps in their current quality management system
  • Strengthen defect prevention and continuous improvement efforts
  • Improve audit readiness and customer compliance
  • Topics covered:

  • Overview of IATF 16949 and automotive industry requirements
  • Process approach, risk-based thinking, and customer-specific requirements
  • Core tools: APQP, PPAP, FMEA, SPC, and MSA Documented information and quality system controls
  • Internal auditing and continual improvement practices
  • Duration:

    14-16 Hours | 2 Days

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Coaching:

    Customized coaching is available.

    Recommended For:

    Quality managers, production supervisors, and internal auditors within the automotive supply chain who need to master the rigorous standards and Core Tools required by global OEMs.

    Contact your Regional Manager to schedule.

    IATF 16949 Internal Auditor Training

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    IATF 16949 Internal Auditor training prepares participants to plan, conduct and report effective audits that support compliance, and continuous improvement in automotive quality systems.

    Participants will:

  • Learn to plan, conduct, and report internal audits effectively
  • Understand IATF 16949 requirements and automotive quality standards
  • Identify nonconformities and opportunities for improvement
  • Apply auditing techniques to assess process effectiveness
  • Strengthen organizational compliance and continuous improvement efforts
  • Topics covered:

  • Overview of IATF 16949 requirements and automotive quality standards
  • Internal audit planning, preparation and execution
  • Audit techniques, checklists and evidence collection
  • Identifying nonconformities and reporting findings
  • Closing audits and supporting corrective actions and continual improvement
  • Duration:

    28-32 Hours | 4 Days

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Recommended For:

    Quality professionals and staff members who are responsible for conducting internal audits to ensure compliance with IATF 16949 and customer-specific automotive requirements.

    Contact your Regional Manager to schedule.

    IATF 16949 Internal Auditor Upgrade Training

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    IATF 16949 Internal Auditor Upgrade Training course prepares experienced auditors to enhance their skills, stay current with automotive quality standards, and effectively lead audits that drive continual improvement.

    Participants will:

  • Update knowledge of the latest IATF 16949 requirements and automotive standards
  • Enhance auditing techniques for more effective assessments
  • Identify nonconformities and improvement opportunities with greater precision
  • Strengthen reporting and corrective action follow-up skills
  • Support organizational compliance and continuous improvement initiatives
  • Topics covered:

  • Updates to IATF 16949 requirements and automotive industry standards
  • Advanced internal audit planning, execution, and reporting techniques
  • Identifying nonconformities and evaluating process effectiveness
  • Corrective action verification and follow-up procedures
  • Best practices for supporting continual improvement and compliance
  • Duration:

    28-32 Hours | 4 Days

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Recommended For:

    Quality professionals and staff members who are responsible for conducting internal audits to ensure compliance with IATF 16949 and customer-specific automotive requirements.

    Contact your Regional Manager to schedule.

    IATF 16949 Technical Assistance

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     IATF 16949 Technical Assistance provides expert-led support to implement the Five Core Tools and develop a robust, process-based management system tailored to their specific automotive manufacturing needs. Our team provides hands-on guidance to close gaps in documentation, satisfy unique OEM requirements, and ensure your facility is fully prepared for a successful certification audit.

    Duration:

    30-32 Days

    Format:

    Customized on-site, in-person assistance

    Contact your Regional Manager to schedule.

    IATF 16949 Internal Audit Services

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    Hiring our team to perform your IATF 16949 Internal Audit ensures an objective, thorough assessment of your quality management system by experienced automotive auditors. Our service helps identify gaps, verify compliance and provide actionable recommendations to drive continual improvement and audit readiness.

    Duration:

    Varies

    Format:

    On-site, in-person audit service

    Contact your Regional Manager to schedule.

    ISO 13485 and ISO 14971 Medical Devices
    ISO 13485 & ISO 14971 Medical Devices

    ISO 13485 and ISO 14971 training provides a comprehensive foundation for medical device manufacturers to align their Quality Management System with international safety and risk standards. This course bridges the gap between general quality principles and the specific regulatory demands of the medical industry.

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    ISO 13485 Overview

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    ISO 13485 training is designed to provide medical device professionals with the essential knowledge to build and maintain a Quality Management System that meets rigorous regulatory requirements.

    Participants will:

  • Understand the key requirements of ISO 13485 for medical device quality systems
  • Learn how to apply risk-based thinking across product and process controls
  • Identify gaps in their current quality management system
  • Gain tools to support regulatory compliance and audit readiness
  • Improve consistency, traceability and product quality across operations
  • Topics covered:

  • Overview of ISO 13485 and regulatory expectations
  • Medical device quality management system requirements
  • Risk management and design & development controls
  • Document control and recordkeeping best practices
  • Internal auditing and continuous improvement processes
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Recommended For:

    Quality, regulatory, engineering, and operations professionals responsible for ensuring medical devices meet regulatory and customer requirements.

    Contact your Regional Manager to schedule.

    ISO 14871 Overview

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    ISO 14971 training course prepares medical device teams to apply risk management principles and confidently meet regulatory and compliance requirements before certification.

    Participants will:

  • Understand the principles and requirements of ISO 14971
  • Learn how to identify, evaluate and control medical device risks
  • Apply risk management throughout the product lifecycle
  • Improve compliance with regulatory and safety expectations
  • Strengthen documentation and audit readiness
  • Topics covered:

  • Overview of ISO 14971 and regulatory risk management requirements
  • Hazard identification and risk analysis techniques
  • Risk evaluation, control and residual risk assessment
  • Risk management file and documentation practices
  • Post-market surveillance and ongoing risk monitoring
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Recommended For:

    Quality, regulatory, engineering, and operations professionals responsible for ensuring medical devices meet regulatory and customer requirements.

    Contact your Regional Manager to schedule.

    ISO 14001 Environmental Management
    ISO 14001 Environmental Management

    ISO 14001 training and services help organizations build and maintain an effective environmental management system. Offerings include an Overview course, Internal Auditor training, Technical Assistance and Internal Audit service to ensure compliance, improve environmental performance and drive continual improvement.

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    ISO 14001 Overview

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    ISO 14001 training course prepares organizations to develop and implement an effective environmental management system that meets international standards and regulatory requirements.

    Participants will:

  • Understand the key requirements of ISO 14001 and environmental management systems
  • Learn how to identify and manage environmental aspects and impacts
  • Apply risk-based thinking to improve environmental performance
  • Strengthen compliance with regulatory and sustainability requirements
  • Support continual improvement and organizational sustainability goals
  • Topics covered:

  • Overview of ISO 14001 and environmental management system requirements
  • Environmental aspects, impacts, and compliance obligations
  • Risk-based thinking and setting environmental objectives
  • Documentation, monitoring and performance measurement
  • Internal audits and continual improvement processes
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Coaching:

    Customized coaching is available.

    Recommended For:

    Professionals responsible for environmental compliance, sustainability initiatives and managing an organization’s environmental management system.

    Contact your Regional Manager to schedule.

    ISO 14001 Internal Auditor Training

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    ISO 14001 Internal Auditor training equips participants with the skills to plan, conduct and report audits that ensure environmental management system compliance and continual improvement.

    Participants will:

  • Learn to plan, conduct, and report effective internal audits
  • Understand ISO 14001 requirements and environmental management principles
  • Identify nonconformities and opportunities for improvement
  • Apply auditing techniques to assess system effectiveness
  • Support compliance, performance improvement and continual environmental improvement
  • Topics covered:

  • Overview of ISO 14001 requirements and environmental management principles
  • Internal audit planning, preparation and execution
  • Audit techniques, checklists and evidence collection
  • Identifying nonconformities and reporting audit findings
  • Closing audits and supporting corrective actions and continual improvement
  • Duration:

    14-16 Hours | 2 Days

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)*

    Recommended For:

    Professionals responsible for auditing, maintaining or improving an organization’s environmental management system.

    Contact your Regional Manager to schedule.

    * Visit our Courses for scheduled open enrollment sessions

    ISO 14001 Technical Assistance

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    ISO 14001 Technical Assistance provides expert guidance to develop, implement and optimize their environmental management system. This service helps ensure compliance, improve environmental performance and supports ongoing continual improvement efforts.

    Duration:

    10-12 Days

    Format:

    Customized on-site, in-person assistance

    Contact your Regional Manager to schedule.

    ISO 14001 Internal Audit Services

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    Hiring our team to perform your ISO 14001 Internal Audit provides an expert, unbiased evaluation of your environmental management system. Our auditors help identify compliance gaps, ensure regulatory adherence, and deliver actionable recommendations to enhance environmental performance and continual improvement.

    Duration:

    Varies

    Format:

    On-site, in-person audit service

    Contact your Regional Manager to schedule.

    ISO 45001 Occupational Health and Safety Management
    ISO 45001 Occupational Health & Safety Management

    ISO 45001 training and services help organizations establish and maintain an effective occupational health and safety management system. Offerings include an overview course, internal auditor training, technical assistance and internal audit support to ensure compliance, improve workplace safety and drive continual improvement.

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    ISO 45001 Overview

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    ISO 45001 Occupational Health & Safety training course equips organizations to implement a robust safety management system that protects employees, ensures regulatory compliance, and supports continual improvement.

    Participants will:

  • Understand the key requirements of ISO 45001 and occupational health & safety management systems
  • Learn to identify hazards and assess workplace risks
  • Apply risk-based thinking to improve safety performance
  • Strengthen compliance with regulatory and legal obligations
  • Support continual improvement and a safer work environment
  • Topics covered:

  • Overview of ISO 45001 requirements and occupational health & safety management principles
  • Hazard identification, risk assessment and control measures
  • Legal and regulatory compliance obligations
  • Setting objectives, monitoring performance and continual improvement
  • Internal audits and safety management system documentation practices
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Recommended For:

    Health, safety and operations professionals responsible for managing workplace safety and occupational health systems.

    Contact your Regional Manager to schedule.

    ISO 45001 Internal Auditor Training

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    ISO 45001 Internal Auditor training equips participants with the skills to plan, conduct and report effective audits that ensure occupational health and safety system compliance and continual improvement.

    Participants will:

  • Learn to plan, conduct and report effective internal audits
  • Understand ISO 45001 requirements and occupational health & safety principles
  • Identify nonconformities and areas for improvement
  • Apply auditing techniques to evaluate system effectiveness
  • Support compliance, risk reduction and continual improvement in the workplace
  • Topics covered:

  • Overview of ISO 45001 requirements and occupational health & safety management principles
  • Internal audit planning, preparation and execution
  • Audit techniques, checklists and evidence collection
  • Identifying nonconformities and reporting audit findings
  • Closing audits and supporting corrective actions and continual improvement
  • Duration:

    14-16 Hours | 2 Days

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)
    * Visit our Courses for scheduled open enrollment sessions

    Recommended For:

    Health, safety and operations professionals responsible for managing workplace safety and occupational health systems.

    Contact your Regional Manager to schedule.

    ISO 45001 Technical Assistance

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    ISO 45001 Occupational Health & Safety Technical Assistance receive expert guidance to develop, implement, and optimize their safety management system. This service helps ensure regulatory compliance, improve workplace safety and supports ongoing continual improvement initiatives.

    Duration:

    10-12 Days

    Format:

    Customized on-site, in-person assistance

    Contact your Regional Manager to schedule.

    ISO 45001 Internal Audit Services

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    Hiring our team to perform your ISO 45001 Occupational Health & Safety Internal Audit provides an objective, expert assessment of your safety management system. We help identify gaps, ensure regulatory compliance and deliver actionable recommendations to enhance workplace safety and drive continual improvement.

    Duration:

    Varies

    Format:

    On-site, in-person audit service

    Contact your Regional Manager to schedule.

    ISO 50001 Energy Management
    ISO 50001 Energy Management

    ISO 50001 Overview training course helps organizations understand and implement an effective energy management system.

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    ISO 50001 Overview

    ISO 50001 Overview training course introduces participants to energy management system principles and prepares organizations to improve energy performance, efficiency and compliance with international standards.

    Participants will:

  • Understand the key requirements of ISO 50001 and energy management systems
  • Learn how to identify and monitor energy use and performance
  • Apply energy management principles to reduce costs and environmental impact
  • Strengthen compliance with regulatory and sustainability standards
  • Support continual improvement in energy efficiency and organizational performance
  • Topics covered:

  • Overview of ISO 50001 requirements and energy management system principles
  • Energy planning, baseline establishment, and performance measurement
  • Identifying energy risks and opportunities for improvement
  • Documentation, monitoring and reporting practices
  • Continual improvement and integration with organizational processes
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Contact your Regional Manager to schedule.

    ISO 17025 Testing and Calibration Laboratories Internal Audit
    ISO 17025 Testing & Calibration Laboratories Internal Audit

    Hiring our team to perform your ISO 17025 Testing & Calibration Laboratories Internal Audit ensures an impartial review of your laboratory’s quality management system. Our experts help identify gaps, verify compliance with international standards and provide actionable recommendations to enhance accuracy, reliability and continual improvement in laboratory operations.

    Contact your Regional Manager to schedule.

    Core Quality Tools
    Core Quality Tools

    Our Core Quality Tools training courses provide comprehensive instruction on essential quality management methodologies, including FMEA, Problem-Solving and Root Cause Analysis, MSA, SPC, APQP, PPAP and Control Plans. Participants gain practical skills to prevent defects, improve processes, ensure product quality and support compliance with industry standards.

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    Failure Mode and Effect Analysis (FMEA)

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    Failure Mode and Effects Analysis (FMEA) is a systematic, step-by-step approach used to identify potential failures, faults and variations in a product, design, or process before they occur. This method is a critical preventive tool for enhancing design and process reliability in occupational health and safety, manufacturing and quality management.

    Participants will:

  • Identify potential failure modes in products, processes and systems
  • Evaluate risk using severity, occurrence and detection ratings
  • Prioritize issues using the Risk Priority Number (RPN) method
  • Develop effective actions to reduce or eliminate high-risk failures
  • Apply FMEA tools to real-world manufacturing and quality challenges
  • Topics covered:

  • Purpose and types of FMEA (Design, Process and System)
  • Identifying failure modes, causes, and effects
    Severity, occurrence and detection rating methods
  • Risk Priority Number (RPN) and risk ranking
  • Developing and tracking corrective and preventive actions
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Recommended For:

    Engineers, quality professionals and operations teams responsible for designing, improving, or managing products and processes.

    Contact your Regional Manager to schedule.

    Problem-Solving & Root Cause Analysis

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    Root Cause Analysis (RCA) is a systematic approach used to diagnose underlying causes of faults, variations and recurring problems within an organization. This course equips participants with practical problem-solving skills to identify, analyze and resolve issues at their source—ensuring long-lasting solutions and improved operational performance.

    Participants will:

  • Apply a structured approach to solving complex problems
  • Identify true root causes using proven analysis tools
  • Use data to validate causes and solutions
  • Develop effective corrective and preventive actions
  • Prevent recurrence of issues across processes and systems
  • Topics covered:

  • Structured problem-solving methodologies
  • Root cause analysis tools (5 Whys, Fishbone, Pareto)
  • Data collection and analysis techniques
  • Corrective and preventive action planning
  • Verification of solution effectiveness
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Recommended For:

    Managers, engineers, and frontline teams responsible for identifying, fixing and preventing operational and quality issues.

    Contact your Regional Manager to schedule.

    Measurement Systems Analysis (MSA)

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    Measurement System Analysis (MSA) is a critical first step before implementing Statistical Process Control (SPC), capability studies, or process improvement initiatives. A reliable measurement system is essential for ensuring accurate, data-driven decisions in manufacturing and quality control.

    Participants will:

  • Understand how measurement systems impact data reliability
  • Evaluate accuracy, precision and bias in measurement systems
  • Perform basic gage repeatability and reproducibility (GR&R) studies
  • Interpret MSA results to support sound decision-making
  • Improve measurement processes to ensure consistent, reliable data
  • Topics covered:

  • Fundamentals of measurement system variation
  • Accuracy, precision, bias, linearity and stability
  • Gage Repeatability and Reproducibility (GR&R) studies
  • Data collection and analysis methods
  • Interpreting MSA results and improvement actions
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Recommended For:

    Quality, engineering, and manufacturing professionals who rely on measurement data to make process and product decisions.

    Contact your Regional Manager to schedule.

    Statistical Process Control (SPC)

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    This one-day hands-on workshop is designed to develop your understanding of key Statistical Process Control (SPC) methodologies within a Quality Management System (QMS). Through group activities and individual participation, you will gain practical experience in selecting, applying and interpreting SPC tools to drive data-driven decision-making and process improvements.

    Participants will:

  • Understand how to monitor and control process variation
  • Use control charts to detect trends and out-of-control conditions
  • Distinguish between common and special cause variation
  • Analyze process performance using SPC data
  • Apply SPC tools to improve quality and process stability
  • Topics covered:

  • Basics of process variation and quality control
  • Control charts for variables and attributes
  • Identifying common cause vs. special cause variation
  • Process capability analysis (Cp, Cpk)
  • Implementing SPC in manufacturing and service processes
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Recommended For:

    Quality, production and process engineers or operators who monitor and improve process performance.

    Contact your Regional Manager to schedule.

    Advanced Product Quality Planning (APQP)

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    Advanced Product Quality Planning (APQP) course provides a structured approach to product and process quality planning to ensure customer satisfaction with new products, process changes and supplier collaboration. With increasingly complex products and supply chains, failures can occur at multiple stages—APQP helps mitigate these risks by providing a standardized framework for communication between customers and suppliers.

    Participants will:

  • Understand the APQP framework and its phases
  • Develop product and process quality plans
  • Identify potential risks and preventive actions early in development
  • Coordinate cross-functional teams to meet quality objectives
  • Apply APQP tools to ensure successful product launches
  • Topics covered:

  • APQP phases and deliverables overview
  • Product design and process development planning
  • Risk assessment and failure prevention strategies
  • Control plans, PFMEA and process documentation
  • Launch readiness and continuous improvement practices
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Recommended For:

    Engineers, quality professionals, and project managers involved in new product development and launch processes.

    Contact your Regional Manager to schedule.

    Product Part Approval Process (PPAP)

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    The Product Part Approval Process (PPAP) course is designed to help organizations establish confidence in their suppliers and production processes by effectively implementing the Production Part Approval Process (PPAP). PPAP defines the approval process for new or revised parts, ensuring that products meet customer expectations and industry requirements.

    Participants will:

  • Understand PPAP requirements and submission levels
  • Prepare and organize PPAP documentation for parts and components
  • Evaluate production processes for compliance and consistency
  • Identify and address issues before part approval
  • Ensure readiness for successful supplier and customer approvals
  • Topics covered:

  • Overview of PPAP purpose and submission levels
  • Required documentation and forms (e.g., Part Submission Warrant, DFMEA, PFMEA)
  • Process and product validation requirements
  • Common pitfalls and corrective actions
  • Supplier and customer approval procedures
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Recommended For:

    Engineers, quality professionals and supply chain personnel involved in part approval and production validation.

    Contact your Regional Manager to schedule.

    Control Plans

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    This one-day course is designed to provide participants with a structured approach to defining the measurements, inspections, quality checks and process monitoring required at each phase of a process to ensure that outputs consistently meet predetermined requirements.

    Participants will:

  • Understand the purpose and benefits of control plans
  • Develop and document effective control plans for products and processes
  • Identify critical process steps and quality characteristics
  • Implement monitoring and measurement strategies to ensure process control
  • Use control plans to support continuous improvement and compliance efforts
  • Topics covered:

  • Purpose and components of a control plan
  • Identifying critical-to-quality (CTQ) characteristics
  • Process flow and inspection point documentation
  • Monitoring, measurement and reaction plans
  • Using control plans for continuous improvement and risk mitigation
  • Duration:

    7-8 Hours | 1 Day

    Format:

    Customized on-site, in-person instruction or Virtual Instructor-led Training (VILT)

    Recommended For:

    Quality, manufacturing, and process engineers responsible for process control and product consistency.

    Contact your Regional Manager to schedule.

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