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ISO 13485 Training & Consulting

Achieve and sustain ISO 13485 certification with training and consulting from

Oriel STAT A MATRIX can help you:

Why Choose Oriel STAT A MATRIX?

Leverage five decades of experience 

Founded in 1968, Oriel STAT A MATRIX has trained more than 130,000 auditors and helped hundreds of organizations regulated by FDA and global regulatory agencies achieve certification to internationally recognized standards such as ISO 9001 and ISO 13485.

Learn from an industry leader in life sciences compliance 

In 1977, FDA chose Oriel STAT A MATRIX to train their investigators in the new draft Good Manufacturing Practice (GMP) regulation, the precursor to the current cGMP/Quality System Regulation (QSR). Oriel STAT A MATRIX worked with FDA to refine the GMP regulations while completing the training of the investigators. Since then, we’ve trained tens of thousands of people in this regulation, as well as subsequent versions, and assisted hundreds of organizations in achieving compliance to these regulations.

Focus on excellence 

By choosing Oriel STAT A MATRIX, you benefit from our experience as a worldwide consultant in quality management and business process improvement. We do not simply conduct ISO 13485 training and consulting; we also show you how to implement the standard as an integral tool to improve your efficiency, productivity, and profitability.

What is ISO 13485?

ISO 13485 is the harmonized quality system standard for medical device manufacturers, their suppliers, and other third parties that provide products or product components, including QMS-related services for the company. ISO 13485 is based on ISO 9001 and supplemented with additional requirements relating to design, special processes, environmental control, traceability, documentation records, and regulatory actions. Unlike ISO 9001, which requires organizations to demonstrate continual improvement, ISO 13485 requires only that an organization demonstrate that the quality system is implemented and maintained.

Who needs to be certified to ISO 13485?

Certification to the ISO 13485 standard is often a prerequisite if you want to sell your medical device and/or IVD outside of the United States. Although being registered does not fulfill the requirements of the various industry regulators, such as US Food and Drug Administration (FDA), ISO 13485 is commonly used as the basis for regulatory requirements. As such, implementation of the ISO 13485 standard is an essential consideration, not only for exporters but also for the local market, global suppliers, and subcontractors to prove that their medical device products are manufactured to the highest quality.

What are some of the key updates for ISO 13485:2016?

ISO 13485 is evolving to keep up with changes in the medical device industry. A revised ISO 13485 was published on February 25, 2016 - the first revision in over a decade.  The changes are comprehensive and include:  

  • A broader focus on risk throughout the standard’s clauses, requiring more senior management involvement in the quality management system
  • Greater supplier controls, including risk-based controls
  • Additional management review requirements
  • The integration of competency with training requirements
  • A focus on requirements for software
  • Validation using preclinical and clinical evaluations
  • Validation of packaging and distribution requirements
  • A feedback section, including a new complaint-handling section and other guidance for customer communications
  • Additional improvement measures: adding the use of postmarket surveillance, risk-based decisions, and timelines

Learn more about the revised standard, read our Market Update or take our training courses Transition to ISO 13485:2016.  

How long do I have to transition to ISO 13485:2016?

  • Before March 2018, organizations may still certify for the first time to ISO 13485:2003.
  • As of March 2019, certifications issued to ISO 13485:2003 will no longer be valid.
  • The expiration date of certifications to ISO 13485:2003 issued during the transition period need to correspond to the end of the three-year transition period in March 2019.

What is the difference between FDA’s QSR outlined in 21 CFR 820 and ISO 13485?

In the US, FDA requires compliance to Quality System Regulation (QSR) – as outlined in 21 CFR 820 – for all medical device manufacturers distributing products via interstate commerce. Conformance to ISO 13485 is voluntary.

However, in the EU and many other countries, conformance to ISO 13485 is often seen as the first step in achieving compliance with those countries’ regulatory requirements. 

Will MDSAP require conformity to ISO 13485?

The MDSAP audit model includes ISO 13485 requirements. There are currently two versions of the audit model: one with ISO 13485:2003 requirements and the other with ISO 13485:2016 requirements.  Note, however, that conformance to ISO 13485:2016 is just one element of meeting the requirements of MDSAP. Learn more.

Will the new EU Medical Device Regulations require EN ISO 13485:2016 certification?

Fundamentally yes. Although the regulations do not require certification to a specific EN ISO standard, medical device companies must establish and implement a quality system that meets a number of compliance requirements outlined in the new Medical Device Regulation and In Vitro Diagnostic (IVD) Regulation.

The easiest way to achieve this compliance is to establish, implement, and attain EN ISO 13485 certification for the manufacturer’s quality management system. EN ISO 13485:2012 is the current harmonized standard for quality systems, as published in the Official Journal. We anticipate that, in a short time, the EN ISO 13485:2016 standard will become the harmonized standard for quality systems, as the presumed conformity for EN ISO certification will need upgrading to the 2016 version by March 2019.

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
Understanding an ISO 13485 Quality Management System
Updated!   Transition to ISO 13485:2016
New!   Transition to the New EU Medical Device Regulation (MDR)
Updated!   Quality Systems for Medical Devices:
FDA’s QSR and ISO 13485:2016
New!   Performance-Based Auditing for Medical Devices
A Tool for FDA’s Case for Quality

Now updated for ISO 13845:2016!  This interactive course gives you the relevant skills and knowledge you need to audit quality management systems for medical devices (QMS). Exercises include audit criteria from 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. Course exercises feature audit criteria from ISO 13485:2016. Click to learn more.

This course is for organizations in the medical device supply chain that are considering gaining ISO 13485:2016 certification or are new to ISO 13485 and want to understand the requirements. Click to learn more.

Learn key changes in ISO 13485:2016 and prepare for your ISO 13485:2016 upgrade audit with this course. 

In this new 2-day course you will learn about the new requirements in the MDR and how to plan an efficient transition. Click to learn more.

Gain a solid understanding of the necessary components of an effective, compliant quality system for medical device manufacturing. Click to learn more.

Designed for experienced auditors. Course participants learn how to go beyond compliance and analyze the performance-related data needed to improve processes, produce higher-quality devices, and achieve better patient outcomes.

Our team is here to help. Call 1.888.532.6360 or contact us online ›