Date: Wednesday 1st February, 2012 - Thursday 2nd February, 2012
Start time: 9:30 AM
Duration: 15 hour(s)
Cost: £1250
Provider: Management Forum
This seminar will take many aspects of animal health and veterinary research and development through a typical clinical trial, and pay attention to compliance with GCP as outlined in the two guidelines on safety and efficacy produced by FEDESA and the CVMP. The meeting will address a typical case study where a practical approach will be made to setting up, running and monitoring clinical trials followed by an audit of these studies to satisfy the stringent requirements seen in Europe. Standard documentation utilised for recording data, performing audits and a typical protocol will be supplied for use in the delegates’ company own laboratories.
Who is it for?
Those responsible for monitoring veterinary clinical studies, setting up protocols and studies, both in the Laboratory and Field environment; Practice guidelines;
Quality Assurance professionals who are required to audit these types of studies;
Clinical Project Managers;
Regulatory Affairs personnel.
The Speakers
Professor George Gettinby is Professor in Statistics, Department of Statistics and Modelling Science, University of Strathclyde.
Sue Lester was a founding Director of
Triveritas and is a leading international expert in Quality Assurance (GCPv,GLP and GMP).
The Venue
The Rembrandt Hotel, 11 Thurloe Place,
London SW7 2RS
Number of CPD hours this event can be recorded as
11 hours
Registration and Booking
Click here to reserve your place