March 10 - 11, 2015    london , United Kingdom
BENEFITS IN ATTENDING:

Understand the regulatory requirements and study design
Know how to design protocols and apply them
Take away practical advice on how to set up clinical trials
Clarify the pharmacovigilance requirements
Gain a better understanding of data handling and appropriate statistics
Discover how to produce the final report
Assure quality in laboratory field studies

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 int he company attendees own laboratories.

Venue

Location: The Rembrandt
Contact 11 Thurloe Pl. Twickenham , United Kingdom

Organizer

Management Forum Ltd
Management Forum Ltd 98-100 Maybury Road, Woking, GU21 5JL
+44 (0) 1483 730071