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ISO 13485 Medical Devices Internal Auditor Training  cover image

ISO 13485 Medical Devices Internal Auditor Training
SGS Academy

Medical Devices internal auditor

Summary

Price
£1,500 inc VAT
Finance options

The cost for this training can be split into interest free repayments. Please contact us for...

Study method
Online + live classes
Course format
Video
Duration
2 days · Full-time
Qualification
No formal qualification
Certificates
  • Certificate of Completion - Free
Assessment details
  • Continuous Assessment (included in price)
Additional info
  • Tutor is available to students

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Dates

Start date
End date
21/05/2026
22/05/2026
04/11/2026
05/11/2026

Overview

This course has been prepared by the medical device specialists of SGS and the content approved by SGS United Kingdom Ltd. SGS United Kingdom Limited is approved as Notified Body 0120, a CMDCAS Recognised Registrar, UKAS accredited certification body 005, under the FDA Approved Persons Program and is recognised by many other regulatory authorities including those in Australia and Taiwan.

Other medical device approvals in the SGS group include SGS Japan Inc as a JPAL Registered Certification Body and SGS Hong Kong Ltd recognised by the Hong Kong Medical Device Control Office.

Certificates

Certificate of Completion

Digital certificate - Included

Assessment details

Continuous Assessment

Included in course price

Resources

  • ISO 13485 Medical Devices Quality Management Systems Internal Auditor Course Synopsis -

Description

The objective of this course is to provide delegates with the skills required to conduct internal audits as required by ISO 13485.

Upon completion of this course delegates will be able to :

Understand the requirements of ISO 13485:2016, and the quality system requirements of Directives 93/42/EEC and 98/79/EC

  • Know how to conduct internal quality system audits
  • Understand the role of internal audit in the maintenance and improvement of management systems
  • Plan and prepare for an internal audit
  • Learn to gather evidence by observation, questioning & sampling
  • Write factual reports on the compliance of the management system against the audit standards
  • Participate in the corrective action process

Who is this course for?

This course is designed to familiarise quality and regulatory professionals, engineers, designers and management with the requirements for internal auditing of ISO 13485 quality systems.

To gain the most from this training, delegates will require a copy of ISO 13485 as it will be reviewed and referred to during the training.

Requirements

Whilst this is an introductory course, delegates are expected to have basic knowledge or awareness of quality management systems, such as one of the previous versions of the ISO 13485 standard. It is advisable to have read the ISO 13485:2016 standard prior to attending the course.

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