MEDICAL DEVICE
CLINICAL STUDIES

Conference Date: 08-09 Dec 2008
Conference Ref: N12-8108
Fee: £1050 + VAT
Venue: The Rembrandt Hotel, London

Introduction

This course has been designed specifically for those involved in conducting medical device clinical investigations and post market studies.  The collection of clinical data to demonstrate safety and performance of a device is pivotal to CE marking.  The collection of post market data is a key aspect of continued safety and performance considerations once the device is on the market.  This course will cover the full range of clinical research activities that should be applied during the collection of data for both pre and post market studies.  It will provide delegates with information on the European regulations for conducting medical device studies and help them to run studies in Europe and other countries.  Delegates should benefit from the advice and tips on the practicalities of conducting studies within Europe.