Medical device clinical studies
MEDV04
Who would benefit?
Those new to medical device clinical studies with some responsibility for setting up, monitoring or managing medical device studies. Study site personnel who have had little experience of conducting medical device studies.
Course Objectives
At the end of the course delegates will be able to:-
- Explain the regulations applicable to medical device studies.
- Define what minimum study documentation is needed.
- Describe the pre-trial procedures and be able to provide an overview of other necessary study procedures.
Programme
This course gives an excellent overview and introduction to device studies and is suitable for those with little experience of conducting medical device studies. The day will include case studies and ample time for discussions:
- The regulatory requirements for conducting medical device studies
- Essential study documentation
- Obtaining approvals and pre-trial procedures
- Study management and monitoring.
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))
