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Training Course on Essentials of Clinical Study Management

 
  January 09, 2011  
     
 
Radisson Blu Alcron Hotel , Prague, Czech Republic
May 18 2011 8:00AM - May 20 2011 3:30PM


All you’ve ever wanted to know about Clinical Study Management... and more
Learn the Ins-and-Outs of Study Management, the Clinical Study Environment, and overall Drug Development.

Featuring an esteemed European training faculty with over 100 years of combined experience in phase I-IV clinical trial management at big pharma, biotechnology firms, CROs and SMEs, as well as academic clinical research centres.

The success of a clinical study is very much dependant on its efficient preparation and effective conduct. Study managers should be knowledgeable about required quality and regulatory standards, roles and responsibilities of team members and be able to select and oversee internal and external resources. Study managers also should be able to anticipate potential problems, offer creative solutions and develop strategies to mitigate risk.

This training course provides a comprehensive overview of the essential elements of study management and the clinical study environment in the context of the overall drug development process. After successful completion of the training course the participants will be able to plan, execute and manage a clinical study from protocol to final report.

 

Event Code:
11537

 

 
 
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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