| One of the aims of EuroPa is to establish
the clinical research and trial organisation for conducting both,
industry-independent and industry sponsored studies. EuroPa members
are in the process of implementing a structure to facilitate,
conduct and manage the various steps of clinical research projects.
Study-independent quality criteria will be developed
by the CREO in order to certify all EuroPa Clinical centers as
“Centers of Excellence” for clinical research trial
participation. This will guaranty quality and sustainability of
EuroPa project research activities.
Responsible persons
CREO EXECUTIVE BOARD
- Prof Olivier RASCOL (Toulouse, France)
- Prof Wolfgang OERTEL (Marburg, Germany)
- Prof Cristina SAMPAIO (Lisbon, Portugal)
CREO SCIENTIFIC ADVISORY BOARD
- W Poewe (Austria)
- E Ruzicka (Czech Republic)
- O Rascol (France)
- W Oertel (Germany)
- R Djaldetti (Israel)
- P Barone (Italy)
- N Leenders (The Netherland)
- C Sampaio (Portugal)
- E Tolosa (Spain)
- H Widner (Sweden)
- A Lees (UK)
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