Event Date/Time: Oct 12, 2009 | End Date/Time: Oct 13, 2009 |
Description
This event is a must for professionals wanting to listen to informed presentations on all aspects of clinical trials, from the orphan drug regulation to the use of modelling and biostatistics in patient recruitment, it will cater for the needs of all people involved in clinical trials.
Why should you attend this event?
IMPROVE understanding of conducting clinical trials in emerging markets
DISCOVER the developments in the uses of statistical modelling
ENSURE compliance with the EU Directive in clinical safety reporting
EXAMINE the developments in patient recruitment
HEAR about the progress of adaptive design in clinical trials
PLUS HALF DAY ASSOCIATED POST-CONFERENCE WORKSHOP
The Safety Aspects of Clinical Trials Reporting in the EU
14th October 2009, Crowne Plaza Hotel - St James, London, United Kingdom
Workshop Host: Graeme Ladds, Director, PharSafer Associates