MEDICAL DEVICE
CLINICAL STUDIES

Conference Date: 23-24 Jan 2013
Conference Ref: N1-8213
Fee: £1255 + VAT
Venue: The Rembrandt Hotel, London

BENEFITS IN ATTENDING:

Participants should expect two extremely informative days with ample time for discussion, questions and case studies.

Delegates will:

• Understand the role of clinical research in device development within the medical device industry
• Discover clinical trials methodology in the preparation and conduct of clinical trials of medical devices
• Take away practical knowledge on how to plan, organise and conduct clinical trials of medical devices successfully

WHO SHOULD ATTEND:

This course will be of value to those who are involved in conducting medical device studies (clinical evaluations, clinical investigations and post market studies) and particularly where data may be used to support the CE marking process. Personnel involved in setting up, managing and monitoring studies will benefit from this seminar, also those involved in research and development, marketing and regulatory would enhance their understanding of device studies by attending this course. It will be of interest to  professionals at all levels either new to device studies or those wishing to update and enhance their current knowledge and skills. It will be particularly useful to those moving from pharma studies to device studies.

If you have any questions please click here to contact Andrea James.