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Fundamentals of Clinical Research Monitoring

 
  August 19, 2011  
     
 
Crowne Plaza de Mexico, Mexico City, Mexico
Sep 2 2011 8:30AM - Sep 3 2011 2:45PM


Interactive lecture and hands-on workshop training methods will provide you with the tools to design and manage clinical studies.

 

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

Event Code:
11920

 

 
 
Organized by: DIA
Invited Speakers: See website for speaker information
 
Deadline for Abstracts: Call contact
 
Registration:

To Register click here http://www.servimed.com.mx/dia2011/registro2.html

 

For detailed program information including faculty and topics, please contact:

Colleen Buckley

Tel. +1-215-442-6108

Email Colleen.Buckley@diahome.org

 

 

E-mail: Colleen.Buckley@diahome.org
 
   
 
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