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Training Course on Advanced GCP Study Monitoring

 
  March 27, 2011  
     
 
Marriott Rive Gauche Hotel, Paris, France
Sep 19 2011 8:00AM - 4:30PM


Clinical Research Monitors perform a critical role in the conduct of a clinical trial. As the primary liaison between the sponsor and the site, the monitor must verify that the clinical trial is conducted according to Good Clinical Practice, the safety and rights of subjects are protected, the Investigational Medicinal Product is handled correctly and the data is of the highest quality. This course will expand and strengthen the monitoring skills of Clinical Research Associates, enabling them to perform their role more proficiently and effectively.

Using case studies, monitors will learn how to handle monitoring problems and proactively manage risks before they become audit findings later. This course includes an invaluable “shared experience session” which will enable colleagues to discuss monitoring challenges they face.

 

Event Code:
11531

 

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

ELISABETHENANLAGE 25, POSTFACH

4002 BASEL

SWITZERLAND

 

TEL.: +41 61 225 51 51 

FAX:  +41 61 225 51 52

E-MAIL: DIAEUROPE@DIAEUROPE.ORG

E-mail: diaeurope@diaeurope.org
 
   
 
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