SAS Radisson Hotel Boulogne , Boulogne-Billancourt (Paris) France
Nov 19 2010 - Nov 19 2010
proficiently and effectively.
This course offers a unique possibility: 3 sessions, plus 1 session with a ‘shared experience session’ to discuss ‘your site monitoring problems’. Key Topics
• Source document/data evaluation
• Electronic source data management
• Risk assessment, handling difficult sites and corrective action plans
• Monitoring challenges: special populations, emerging markets Learning Objectives:
At the conclusion of this course participants should be able to:
• Identify risks that would lead to potential fraud cases
Target Audience:
Pharmaceutical, biotechnology and medical device industry
• Freelancers, self-employed
• Orientated towards the needs of CRAs with, say 2 – 3 years experience in the job who want to acquire advanced monitoring skills and/or refresh existing ones.
• Experienced CRAs
• Contract Research Organizations Event Code:
10561
• Study coordinators, interested in monitoring from the sponsor’s perspective
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