Regulatory Reliant Internal Auditing for Medical Devices

97% Recommended

Regulatory Reliant Internal Auditing for Medical Devices is for existing Internal or Lead Auditors seeking the knowledge & skills to perform internal audits based on integrating ISO 13485, MDSAP and FDA QMSR requirements.

Under Regulatory Reliance models, regulators increasingly depend on the effectiveness of your quality system and the credibility of your internal audit programme to inform audit outcomes, inspection scope, and regulatory confidence.

Many organizations discover this the hard way when internal audits pass, yet MDSAP nonconformities escalate, where FDA inspections uncover gaps that should have been caught internally and when Audit Programmes exist, but do not withstand regulatory scrutiny.

This course is designed for organizations that recognize that internal auditing is now a regulatory control, not a compliance formality. Our live learning methodology focuses on practical ‘learn by doing’ workshops set in a real life context.

Regulatory Reliant Internal Auditing for Medical Devices
Trusted By Notified Bodies & Global Brands
Trusted By Notified Bodies & Global Brands
Trusted By Notified Bodies & Global Brands
Trusted By Notified Bodies & Global Brands
Trusted By Notified Bodies & Global Brands
Trusted By Notified Bodies & Global Brands
 
Course Snapshot
Approved By
Comply Guru
Duration
16hrs
Teaching Format
Live Learning
Delivery Options
Virtual or In-Person Workshops
Course Entry Requirements
Prior knowledge is required
Certification on Completion
Issued in 1 business day
Course Content Based on
ISO 13485, MDSAP (v10) and FDA QMSR
Course Last Updated
March 2026
Language (s)
English
Group or In-House Pricing Have 5 or more?

Need Corporate, In-House or Customized Training?

Comply Guru offers corporate, in-house and customized training solutions for your organization’s specific needs.

Speak with an experienced member of our team today to learn how we can help.

How TÜV SÜD utilized eLearning & saved 40% on Lead Auditor Training

FEATURED CUSTOMER

How TÜV SÜD utilized eLearning & saved 40% on Lead Auditor Training

"Comply Guru’s trainers are not only experienced in their specific fields but are also experts in the art of training. By using a provider who integrates modern self-study e-learning methods with traditional in-person sessions, we can be confident that our learning outcomes are maximized."

Zoran Klaric

Manager Regional Training & Onboarding

How Skeletal Dynamics switched to Online Learning & saved 50% on MedTech QARA Training

FEATURED CUSTOMER

How Skeletal Dynamics switched to Online Learning & saved 50% on MedTech QARA Training

“Over the years, I have used many well-known U.S training providers, but I found Comply Guru had truly mastered ‘online’ training which has saved Skeletal Dynamics over 50% in training fees, associated expenses as well as 100% of the time lost spent travelling to training with other providers.”

Mario Arbesu

VP of Quality Assurance & Regulatory Affairs

How Comply Guru helped X-Bolt Trauma Orthopedics add real value to their Quality System

FEATURED CUSTOMER

How Comply Guru helped X-Bolt Trauma Orthopedics add real value to their Quality System

“Comply Guru took the stress out of training. Their courses didn’t just tick a box—they added real value to our quality system.”

Bernard Wallace

Quality Affairs Manager

Course Overview

Regulatory Reliant Internal Auditing for Medical Devices

Key Features Covered
Live Learning from Anywhere
Up-to-date Technical Content & Examples
Practical Case Studies based on Real-World Scenarios
Practical Workshops led by Experienced Lead Auditors
Learning Objectives Covered

Conduct integrated internal audits across ISO 13485, MDSAP, and FDA QMSR

Identify and document regulatory critical audit findings

Perform risk-based audit planning and execution

Generate inspection ready audit reports and follow up actions

Operate an internal audit programme aligned with regulatory reliance

Course Certification

Upon successful completion, each Learner shall receive a digital Certificate of Achievement.

What Are The Entry Requirements

Prior to attending this course, learners are expected to have the following prior knowledge:

  • A working knowledge of ISO 13485:2016
  • An understanding of the MDSAP audit model and requirements
  • Working knowledge with the FDA Quality System Regulation (21 CFR Part 820) and/or QMSR
  • Prior recognized training in internal or lead auditing (e.g. ISO 13485 Internal Auditor or Lead Auditor course)
  • Experience working within a Medical Device Quality Management System (MD-QMS)
How Will You Be Assessed

To successfully complete this course, each Learner will need to:

  • Fully attend the Instructor Workshops as 100% attendance is required.
  • Obtain 70% or higher in the graded assessments during the Instructor Workshops
What Are The Technology Requirements

For the live workshops during a virtual delivery, we utilize Microsoft Teams.

Learners need to individually have:

  • PC or MAC Computer
  • Reliable Internet
  • Video Webcam
  • Headset or Earbuds
  • Quiet Setting

In relation to the eLearning Modules, in our experience, Workplace IT environments’ internal configurations and available software can vary (new or old), and there may be various limitations or other restrictions in place, and as such, the functionality of any Learning Management System (LMS) may be impacted, restricted and may not perform well. Read the full technology requirements here.

Our Methodology

No More Death By PowerPoint

Our courses are designed with practical exercises that have Learners working with scenarios, case studies and material that is focused on a ‘learn by doing’ approach.

No More Death By PowerPoint
No More Death By PowerPoint
 

Course Structure Explained

Agenda Overview

Attend live, instructor-led workshops emphasizing practical, real-world application.

Time Topic
Topics Covered
  • Regulatory Reliance & the Role of Internal Auditing
  • Integrating ISO 13485, MDSAP & QMSR
  • Risk Based Internal Audit Planning
  • Process Based Auditing in a Regulatory Context
  • Regulatory Critical Process Auditing
  • Conducting Integrated Internal Audits
  • Internal Audit Outputs as Regulatory Evidence
  • Auditor Competence, Behaviour & Independence
  • Sustaining a Regulatory Resilient Audit Programme

Our Experts

Meet the Instructors

Our experts possess a wealth of industry experience acquired over years of practical application, and in addition, they demonstrate a combination of unwavering passion and a proven aptitude for training.

Michelle Keane

Our Instructor

Michelle Keane

Michelle has a proven track record with over 20 years of experience working across both the Medical Device and Biotechnology sectors. Currently, she is a Lead Auditor for an INAB Accredited Certification Body, and an MDR Assessor for a Notified Body in Europe. In addition, she is the Team PRRC Representative for Ireland.

About our Internal Auditor Training

Learn about the benefits and key features of Comply Guru’s Instructor led Learning.

 
Why Choose Instructor led Learning

Frequently Asked Questions

Yes, we offer in-house training and if you have 5 or more learners that can be trained together, we strongly recommend arranging for in-house training. With this option, there is the possibility of customizing some elements of the training to your organization. Please request a quote and a member of our team will be in touch to discuss this further with you.
We keep our classes to 10 or 12 maximum depending on the blended course, to ensure you can enjoy breakout rooms, activities and Q&As with the Instructor and other participants.
The fastest and easiest way to pay would be to use your credit card. If you cannot do that, and you require a PO, please email our team at training@complyguru.com
Once you have completed the final assessments, your certificate will be available within 1 business day via your Dashboard. To access your certificate, you must first submit a short course survey and then the certificate will be available for download/print.