Post Market Surveillance Of Medical Devices

MEDV07 - November 11 2012

Who would benefit?

All those who are involved in collecting post-market surveillance information and/or conducting post market surveillance studies for devices which are approved for market.

Course Objectives

At the end of the course delegates will be able to:-

Understand what PMS involves and what guidelines and regulations to apply to PMS.
How to choose which method of PMS is appropriate.
How to develope a PMS protocol.

Programme

This one day practical course will look at the need for post market surveillance of devices and how it can be effectively conducted:-

What is PMS and what does it involve?
What regulations and guidelines exist for conducting PMS?
How should PMS be conducted, the different types of studies and procedures for obtaining PMS data.
Writing the perfect protocol for a PMS study.

Training course booking form

Microsoft Word .doc - Click here to download
Adobe Acrobat .pdf - Click here to download

The form contains the prices and terms & conditions. Please return the completed form either:

As an attachment e-mailed to enquiries@medvance.co.uk,
By fax: +44 (0)1757 270055
By post to: Medvance Ltd, Medvance House, Burn Grange, Doncaster Road, Burn, Selby, North Yorkshire, YO8 8LA, United Kingdom

(NB: Please note that .pdf can only be printed, and then faxed or posted, and not re-edited. Some users may need to right click on the above links and click 'Save target as...'. In order to open/view PDF documents you will need Adobe Reader software installed which can be obtained free from Adobe's Website (click here))