COURSE OBJECTIVES

To covers the key steps of the entire life cycle of a clinical trial from inception to dissemination.

MAIN TOPICS

• Protocol development – 4h Maria Grazia Valsecchi (2h) + Silvia Mori (2h)
• End Point – 2h - Stefania Galimberti
• End point Surrogate – 2h - Giulia Capitoli
• Organizing Data & Data Management, Case report form & ECRF – 6h - Davide Gaudesi
• Safety issues – 2h - Silvia Mori 
• Safety data analysis – 4h – Elena Tassistro
• Practical Review (Def. of a protocol) – 14h – Emanuela Rossi 
• Reporting results – 2h - Francesca Graziano
• Review-meta analysis – 4h - Anita Andreano