Medical Devices Training

Medical Devices Training - ISO 13485

Effective quality management systems are recognized as a key regulatory consideration for allowing medical device manufacturers to market their products around the world. ISO 13485 provides a focus for the quality management system requirements for medical device manufacturers.

BSI can provide training to help you implement a successful Medical Devices Management System. You can choose whether you would like to attend one of our scheduled open courses or have it delivered on your premises as an in-company solution.

Understanding Medical Devices Management Systems - ISO 13485

Gain an understanding of the ISO 13485:2003 Quality Management Systems requirements as well as an introduction to the concepts of ISO 14971 - The Medical Device Risk Management Standard.

Read more details   Read more details

ISO 13485 Internal Auditor

Learn how to apply the principles of the standards to produce effective internal audits of medical device manufacturing firms.

Read more details   Read more details



Training Worldwide

This website contains courses across Continental Europe, Middle East & Africa. Alternatively, you can select a specific country website from below.


Standards & Publications

Review and purchase Medical Devices Standards & Publications from British Standards.


Contact Us

Tel: +44 (0)20 8996 6325
Fax: +44 (0)20 8996 7852
Email: international@bsigroup.com

BSI Group, 389 Chiswick High Road, London, W4 4AL. Email: international@bsigroup.com
© 2007 BSI. Legal Notice.