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ISO 9000 & Related Standards

Go beyond conformance.

Since 1990, we have trained more than 120,000 auditors and helped more than 1,500 organizations attain registration to ISO 9000 and related standards. Our approach ensures organizations use the certification process to optimize productivity, efficiency, and profitability.

Get ready for the new version of ISO 9001 with our new training course,
Transition to ISO 9001:2015.

Our flexible management systems consulting and training services can help you:

Consulting services for management systems compliance and certification

Expect more than compliance to a standard. Oriel STAT A MATRIX is a leading global consultant in Performance Excellence, and we share this expertise in all of our consulting engagements. We help our clients integrate the required compliance activities into their continual improvement processes, so they can improve both quality and results going forward.

Training for management systems compliance and certification

Access the training you need at public training sessions in cities around the U.S., or we can bring any course to your site (recommended for groups of five or more). All of our courses can be customized for your organization.

Why Choose Oriel STAT A MATRIX?

Since 1968, organizations have relied on Oriel STAT A MATRIX for management systems training and consulting. We have trained more than 120,000 auditors and helped thousands of organizations attain certification to ISO 9000 and related management standards, including AS9100, ISO 13485, ISO/TS 16949, and ISO 14000.

Oriel STAT A MATRIX was:

  • The first U.S.-based consultancy to provide ISO 9000 certification consulting (1988).
  • The first U.S.-based trainer to be registered by the Institute of Quality Assurance (IQA) (IRCA predecessor) to train ISO 9000 lead auditors (1990).
  • The first training provider certified by the Registrar Accreditation Board (RAB) (RABQSA predecessor) to offer lead auditor and internal auditor training (1992).

Select a standard to learn more or find a training course:

Select a course below to learn more or to register.
 
Course Name Public On-site
ISO 13485 Lead Auditor Training
ISO 13485 Internal Auditor Training
New!   Transition to ISO 13485:2016
Advanced Lead Auditor Training
ISO 9001 Internal Auditor Training
ISO 9001 Lead Auditor Training
New!   Risk Management for ISO 9001:2015
Statistics for Lead Auditors
New!   Transition to ISO 9001:2015
Quality Systems for Medical Devices: FDA’s QSR and ISO 13485

This interactive course covers ISO 13485 and gives you the relevant skills and knowledge you need to carry out audits of Quality Management Systems for Medical Devices (QMS). Includes an introduction to ISO 13485:2016. Click to learn more.

Exemplar Global Certified QMS Internal Auditor Training Course. Learn the steps to develop, implement, and audit an internal quality system that efficiently and effectively meets the requirements of ISO 13485 and ISO 9001. Includes an introduction to ISO 1385:2016. Click to learn more.

Get up to date with the changes and how they impact your organization.

Learn the skills and knowledge required for a performance-based approach to auditing that will help your organization meet its strategic goals and make your audit program the catalyst for tangible improvement to your organization’s bottom line? Click to learn more.

Understand the steps in developing, implementing, and auditing an internal quality system that meets the requirements of ISO 9001 and the needs of your organization. Click to learn more.

Our ISO 9001 Exemplar Global-certified auditor/lead auditor training course, presented largely through hands-on workshops, teaches you the skills you need to plan, conduct, and follow-up on ISO 9001 compliance audits. Click to learn more.

Based on ISO 31000:2009, Risk management – Principles and guidelines, this course provides a framework for managing risk regardless of the size of the organization, its context, or its industry sector.Click to learn more.

Lead auditors - go beyond conformance with training that shows you how to use statistical knowledge to analyze process data and draw meaningful conclusions. Click to learn more.

In this course, we discuss the major changes that were introduced in the new standard, and address how organizations should consider these changes as opportunities to make their quality management system a strategic element of good performance and sustainability over time. Click to learn more.

Designed for both new and experienced professionals in the medical device field, this course will give you a solid understanding of the necessary components of an effective, compliant quality system for medical device manufacturing. Includes coverage of ISO 13485:2016. Click to learn more.