ISO 13485 Medical Devices Internal Auditor Training
Medical Devices internal auditor
SGS Academy
Summary
- Certificate of Completion - Free
- Exam(s) / assessment(s) is included in price
- Tutor is available to students
Add to basket or enquire
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
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.
Questions and answers
Reviews
Currently there are no reviews for this course. Be the first to leave a review.
Legal information
This course is advertised on Reed.co.uk by the Course Provider, whose terms and conditions apply. Purchases are made directly from the Course Provider, and as such, content and materials are supplied by the Course Provider directly. Reed is acting as agent and not reseller in relation to this course. Reed's only responsibility is to facilitate your payment for the course. It is your responsibility to review and agree to the Course Provider's terms and conditions and satisfy yourself as to the suitability of the course you intend to purchase. Reed will not have any responsibility for the content of the course and/or associated materials.