Scheda insegnamento

Anno Accademico 2020/2021

Conoscenze e abilità da conseguire

Identify key parameters for risk/benefit assessment of drug therapies. Understand sources of variability in clinical drug responses (including pharmacogenomics). Describe the basic methodology of pre-clinical and clinical drug trials, their regulatory and ethical implications, and procedures for marketing authorization, with special reference to biotechnological drugs. Present therapeutic options (conventional and biotech drugs) in the context of a given disease, highlighting innovative aspects. Critically evaluate research articles presenting pre-clinical and clinical data, through consultation of specific databases and documentation provided online by regulatory agencies.


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Metodi didattici

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Modalità di verifica dell'apprendimento

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Strumenti a supporto della didattica

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Orario di ricevimento

Consulta il sito web di Roberto Rimondini Giorgini

Consulta il sito web di Emanuel Raschi