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ISO 13485 Internal Auditor Course

In this free online course, you’ll learn everything you need to know about ISO 13485, but also how to perform an internal audit in your company. This ISO 13485 Internal Auditor course is made for beginners in medical device management system and internal auditing, and no prior knowledge is needed to take this course. If you like this course, you can go for the certification exam. After passing the exam, you will receive a certificate proving that you attained Medical Device Management Systems and Management Systems Auditing competencies.

The course is organized into 9 modules, where each module has several video lectures and quizzes that will help you learn more quickly, as well as a recap quiz that will prepare you for the certification exam – please see below for the content of each module. All the video lectures are pre-recorded, so you can take the course from anywhere, at any time for your convenience.

  • The total course duration, including the reading of required materials, is approximately 15 hours.
  • Materials provided in the course (video lectures, articles, and activity questions) are everything you need to successfully pass the certification exam.
  • There is no time limit for taking the course, but it is recommended that you finish it within two weeks’ time.
  • Access to this course and the quizzes is completely free; the fee for the certification exam is US$ 449 – after you pass the exam, you’ll receive your certificate in a matter of days.

After you purchase the exam, you will receive the completely free ISO 13485 Internal Audit Checklist document and a bonus PDF containing scripts from all of the video lectures and quizzes, links to additional reading, and access to the practice exams.

Course Curriculum

Introduction
Introduction to the course 00:00:00
Module 1 - Introduction to ISO 13485
Introduction & suggested reading 00:00:00
What is ISO 13485:2016? 00:00:00
What is the QMS? 00:00:00
Why is ISO 13485:2016 important? 00:00:00
What is the structure of ISO 13485? 00:00:00
Key principles of quality management 00:00:00
Key interested parties in ISO 13485 00:00:00
Implementing ISO 13485 using The Plan Do Check Act Process 00:00:00
The ISO 13485 Project 00:00:00
Certification FAQs 00:00:00
Recap quiz 00:00:00
Module 2 - Management and Supporting Processes
Introduction & suggested reading 00:00:00
What is a process? 00:00:00
Top management commitment (clauses 5.1 and 5.2) 00:00:00
Quality Policy and objectives (clauses 5.3 and 5.4) 00:00:00
Roles and responsibilities (clause 5.5) 00:00:00
Management review (clause 5.6) 00:00:00
Documentation process (clauses 4.1 and 4.2) 00:00:00
Quality Manual (clause 4.2.2) 00:00:00
Medical Device File (clause 4.2.3) 00:00:00
Handling the QMS documentation (clause 4.2.4) 00:00:00
Records for the QMS (clause 4.2.5) 00:00:00
Importance of Resources management process (clause 6.1) 00:00:00
Managing human resources (clause 6.2) 00:00:00
Managing infrastructure resources (clause 6.3) 00:00:00
Managing work environment (clause 6.4.1) 00:00:00
Managing contamination (clause 6.4.2) 00:00:00
Managing monitoring and measuring equipment (clause 7.6) 00:00:00
Related documentation 00:00:00
Recap quiz 00:00:00
Module 3 - Product Realization Planning, Contract Review, and Design & Development
Introduction & suggested reading 00:00:00
Planning of Product Realization (clause 7.1) 00:00:00
Example of planning Product Realization 00:00:00
Overview of Customer-Related processes (clause 7.2.1) 00:00:00
Review of a contract or customer purchase order (clause 7.2.2) 00:00:00
Communication methods for the Customer-Related processes (clause 7.2.3) 00:00:00
Design and development overview (clause 7.3.1) 00:00:00
Planning for design and development (clause 7.3.2) 00:00:00
Design and development inputs (clause 7.3.3) 00:00:00
Design and development outputs (clause 7.3.4 and 7.3.5) 00:00:00
Design and development verification and validation (clause 7.3.6 and 7.3.7) 00:00:00
Design and development transfer to production (clause 7.3.8) 00:00:00
Control of design and development changes (clauses 7.3.9, 7.3.10) 00:00:00
Related documentation 00:00:00
Recap quiz 00:00:00
Module 4 - Purchasing, Production, and Service Provision
Introduction & suggested reading 00:00:00
Purchasing overview (clause 7.4) 00:00:00
Vendor Evaluation and performance (clause 7.4.1) 00:00:00
Purchasing information and verification of product (clauses 7.4.2 and 7.4.3) 00:00:00
Production and service provision overview (clause 7.5.1) 00:00:00
Qualification of your infrastructure (clauses 7.5.3 and 7.5.6) 00:00:00
Validation of processes (clauses 7.5.6 and 7.5.7) 00:00:00
Labeling and packaging (clause 7.5.11) 00:00:00
Cleanliness of product (clauses 7.5.2 and 7.5.5) 00:00:00
Identification and traceability (clauses 7.5.8 and 7.5.9) 00:00:00
Customer property and preservation (clauses 7.5.10 and 7.5.11) 00:00:00
Post-delivery processes (clauses 7.5.3 and 7.5.4) 00:00:00
Related documentation 00:00:00
Recap quiz 00:00:00
Module 5 - Measurement, Analysis, and Improvement
Introduction & suggested reading 00:00:00
Monitoring and measuring overview (clause 8.1) 00:00:00
Monitoring and measurement of products (clause 8.2.6) 00:00:00
Monitoring and measurement of processes (clause 8.2.5) 00:00:00
Feedback (clause 8.2.1) 00:00:00
Complaint handling (clause 8.2.2) 00:00:00
Reporting to regulatory authorities (clause 8.2.3) 00:00:00
Internal audits (clause 8.2.4) 00:00:00
Control of non-conforming product (clause 8.3) 00:00:00
Analysis of data (clause 8.4) 00:00:00
Improvement (clause 8.5.1) 00:00:00
Corrective actions (clause 8.5.2) 00:00:00
Preventive actions (clause 8.5.3) 00:00:00
Recap quiz 00:00:00
Related documentation 00:00:00
Module 6 - Introduction to the internal audit
Introduction & suggested reading 00:00:00
Internal vs. external audit 00:00:00
The main purpose of the internal audit 00:00:00
ISO Requirements for internal audits 00:00:00
Criteria for selecting the internal auditor 00:00:00
The audit findings 00:00:00
Nonconformities 00:00:00
Observations 00:00:00
Major and minor nonconformities 00:00:00
Related documentation 00:00:00
Recap quiz 00:00:00
Module 7 - Organizing the internal audit
Introduction and suggested reading 00:00:00
Organizing the internal audit 00:00:00
Internal audit procedure 00:00:00
Annual audit program 00:00:00
Audit plan for an individual audit 00:00:00
Related documentation 00:00:00
Recap quiz 00:00:00
Module 8 - Internal audit elements
Introduction and suggested reading 00:00:00
Internal audit elements 00:00:00
Document review 00:00:00
Creation of the checklist 00:00:00
Internal audit report 00:00:00
Corrective action requests and corrective action follow-up 00:00:00
Related documentation 00:00:00
Recap quiz 00:00:00
Module 9 - The main audit
Introduction and suggested reading 00:00:00
Auditor assumptions 00:00:00
Techniques for finding evidence 00:00:00
Sampling the records 00:00:00
Recording the evidence 00:00:00
Interviewing techniques 00:00:00
Remote audits 00:00:00
Auditing integrated management systems 00:00:00
Related documentation 00:00:00
Recap quiz 00:00:00
Instructions for taking the exam and obtaining the certificate 00:00:00

Benefits of getting the certificate

The certificate of competence proves that you attended the eTraining course, and that you passed the exam. This ensures that you understand and can apply the knowledge you gained in each of the course's modules.

How to get certified?

It's simple:
1) Watch complete videos of all lectures, and answer all practice exams.
2) Pass the online certification exam.

Bonuses with the certificate

Once you purchase the certificate, you will receive the following bonuses:

Discount badge

Internal Audit Checklist (Word document)

The purpose of this document is to provide a list of questions in order to help perform an internal audit against ISO 13485. For each clause or control from the standard, the checklist provides one or more questions that should be asked during the audit in order to verify the implementation.

Course Script (PDF)

If you decide to purchase the exam, you will get the PDF script from the course completely free. The script includes everything said in the videos and all quizzes.

This way, you can access course materials any time you like, making it much easier to practice and prepare for the exam.

Free exam retake

Once you purchase the exam, you will be able to retake it.

This means, if you do not pass the exam on your first attempt, you can retake it one time, free of charge.

There is no mandatory waiting period between the two attempts.

Practice Exam

With the purchase of the exam, you get access to practice exams. You can use these exams to test your knowledge and familiarize yourself with the exam environment.

The results from the practice exam do not have any effect on the results of the final exam.

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Frequently Asked Questions

No, you can attend the course as long as you like; however, you should try to finish it in a couple of weeks because otherwise, you won’t get enough benefits out of it.

You can access it any time – the course is a combination of recorded video lectures, quizzes, reading, and other activities, and because all those materials are readily available, you can access them at a time that is convenient for you.

None. The course was made in such a way that a beginner in this topic can easily understand it.

Well, we have to make money somehow :). We have made most of the course freely available, but to access the exam and get the certificate you’ll have to pay a fee – by the way, this fee is by far smaller than the fee for attending the classroom-type course. Additionally, when you pay for the certificate, you will be able to download a PDF scripts from all of the video lectures, activity questions, practice exams, and links to additional reading. This way, you can access the content from the course and prepare for the exam much more easily.

The exam, as well as the whole course, is completely done online, from your office, your home, or any other place convenient for you. For the exam we use an online proctoring service – click here to learn more.

After you finish attending the course, you can go for the exam – if you finish this exam successfully, i.e., if your score is above the minimum, then you will receive the certificate. By the way, during the exam we use an online proctoring service that will ask for proof of your identity, and make sure that you have taken the exam with no external help. Click here to learn more about online proctoring.

The course is a combination of recorded video lectures, quizzes, reading, and other activities – the course takes you through all these materials in an optimal way.

You can access the course using your PC, Mac, or mobile device, using any major browser (i.e., Chrome, Mozilla, Internet Explorer, Safari); a broadband Internet connection will also be needed. And, of course, enough time to attend the course.

The materials provided in the course – recorded video lectures, quizzes, readings, practice exams, and other activities – are everything you need to successfully pass the exam and obtain the certificate. The best part is: they are completely free with unlimited access!

If you decide to purchase the exam, you will receive a bonus PDF containing scripts from all of the video lectures, quiz questions, links to additional reading, and access to the practice exams. This way, you can prepare for the exam much more easily.

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