Quality Systems for Medical Devices

Aims
On completion, participants will:

• understand the requirements of ISO 13485
• understand the quality system requirements of EC Directive 93/42/EEC
• be able to apply this knowledge to their own quality system.

Profile
This intensive two day non-residential course is designed to transfer detailed information about

ISO 13485 and the directive through lectures from medical device lead auditors regularly undertaking notified body audits. Workshops and interactive sessions encourage participants to share experiences and discuss problems relevant to their organisations.

If you book this course along with the MD2 Quality Systems for Medical Devices training course you pay £704+VAT as a special package deal. This helps you make a saving of £176 per person! Call our customer service team on +44 (0)1276 697 777 to find out more.