home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
  HUM-MOLGEN -> Events -> Courses and Workshops  

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.



     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:


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

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
home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap

Generated by meetings and positions 5.0 by Kai Garlipp
WWW: Kai Garlipp, Frank S. Zollmann.
7.0 © 1995- HUM-MOLGEN. All rights reserved. Liability, Copyright and Imprint.