Fundamentals of Clinical Research Monitoring
Venue: Crowne Plaza de Mexico
Location: Mexico City, Mexico
Event Date/Time: Sep 02, 2011 | End Date/Time: Sep 03, 2011 |
Description
Overview
• Good Clinical Practices (GCP)
• Clinical research methodology and its role in drug development
• CRA’s role in clinical research
• Monitoring clinical trials to ensure valid and useful study data
• Basic protocol development
Learning Objectives:
At the conclusion of this course, participants should be able to:
• Describe the basic clinical research elements in drug development
• Recognize the basic elements of clinical trial methodology in the conduct of clinical studies
• Identify and select qualified clinical investigators
• Recognize the requirements for safety surveillance
• Recognize the elements of protocol development
Target Audience:
• Clinical research associates and clinical study monitors with less than two years of experience
• Administrative support personnel
• Study support personnel
Event Code:
11920