ISO 13485:2016 Lead Auditor, Exemplar Global Certified

Course Summary

This course is designed for individuals who are responsible for planning and scheduling an audit program for ISO 13485 and those who must perform audits to ISO 13485.

Upcoming Events

Event Details

32 hours

Combination lecture and individual/group exercises
Available virtually

Description

This course prepares you to perform effective audits of Medical Device Quality Management Systems.  You’ll learn how to interpret the verbiage of the 13485 Standard and apply it to your own organization.  We also cover the requirements of 21 CFR 820, the federal regulations governing medical device management systems.  We’ll take you through the full audit process, including: audit planning and preparation, opening meetings, document review, interviewing auditees, closing meetings and reporting as defined in ISO 19011.  Training includes easy-to-use tools to simplify the auditing process.

This is a practical, how-to course that is not bogged down in academic discussions.  We use case studies, role-plays, and other real-life practice exercises to keep the training active and build competence.

This is a four-day, instructor-led, course. There are written tests on each of the competency units on days 2, 3, and 4. Days 1 and 2 will cover medical device auditing along with a corresponding competency exam (MD). Day 3 will cover management systems auditing (AU) along with a corresponding competency exam. Day 4 will cover lead auditor requirements with a competency exam (TL).

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Who Should Attend

This course is designed for individuals who are responsible for planning and scheduling an audit program for ISO 13485 and those who must perform audits to ISO 13485, including: Quality Assurance Managers, Quality Assurance Professionals, ISO Project Managers, ISO Project Team Members, Compliance Managers, Regulatory Personnel, or anyone desiring an in-depth understanding of the ISO 13485 Audit Process. This course has been specifically designed to meet the needs of the Medical Device Industry.

Learning Objectives

Through training, participants will learn to:

  • Fully understand and interpret the requirements of ISO 13485
  • Understand the requirements contained in 21 CFR 820 and be able to compare these to the requirements in ISO 13485
  • Conduct a practical audit exercise to 21 CFR 820 to ensure understanding of these requirements
  • Understand how to apply the requirements of the ISO 13485 Standards during 5 practical audit exercises conducted during the class
  • Understand the terminology of ISO 13485 and how these apply in a Medical Device Environment
  • Apply the fundamentals of ISO 19011 to master the auditor skills required for an effective and efficient audit
  • Ask audit questions that get results
  • Conduct opening and closing meetings that have impact
  • Construct effective audit checklists
  • Generate effective corrective actions
  • Write the audit report and take corrective action
  • Prepare Audit report
  • Audit Follow-Up

Course Outline

Day 1

  • Course introduction
  • History of Quality Management
  • In-depth Review of the Standard
  • Exercise: Audit Case Studies

Day 2

  • Learning Game on Pre-assignment
  • Test on Standard / Review test
  • Review 21 CFR 820 & Exercise
  • AU Module – Part 1. Intro to Auditing
  • Test on Part 1 / Review Test
  • Part 2. Preparing for an Audit

Day 3

  • Test on Part 2 / Review Test
  • Part 3. Conducting the Audit
  • Test on Part 3 / Review Test
  • Audit Role Play Exercise 1
  • Part 4. Completing the Audit
  • Test on Part 4 / Review Test
  • Exercise: Writing Audit Findings

Day 4

  • TL Unit: Leading an Audit Team
  • Audit Role Play Exercise 2
  • Exercise: Conducting a Closing Meeting
  • Writing the Audit Report
  • Test on TL Unit / Review Test
  • Class Wrap-Up

Prerequisites

All students are required to bring their own printed copy of ISO 13485:2016. Most students will be able to obtain a copy from their company.

Instructors

FAQ

What transferable skills will I gain from this workshop?

By completing this course, you will develop expertise in lead auditing, regulatory compliance, supplier auditing, and risk management, specifically for medical device quality management systems in compliance with ISO 13485:2016.

What other Quality Management courses does QSG offer?

QSG offers a variety of Quality Management System (QMS) training programs, including ISO 9001, IATF 16949, and ISO 17025.

What if I want to customize this course for my company?

We offer customized ISO 13485 Lead Auditor training tailored to your organization’s requirements. Contact us at info@qualitysupportgroup.com for details.

Will I receive a certificate after completing this course?

Yes! Upon successfully completing the course and passing the final exam, participants will receive an Exemplar Global Lead Auditor certification, demonstrating their proficiency in ISO 13485:2016 auditing.

How can I register for this course?

You can register online by selecting your preferred course dates and completing the enrollment process.

How can I become a QSG member and receive discounted training?

QSG members receive exclusive discounts on training programs.

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General FAQ 2

Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry's standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book. It has survived not only five centuries, but also the leap into electronic typesetting, remaining essentially unchanged. It was popularised in the 1960s with the release of Letraset sheets containing Lorem Ipsum passages, and more recently with desktop publishing software like Aldus PageMaker including versions of Lorem Ipsum.

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