Informed Consent

All health interventions require the patient's specific and free consent, having been notified beforehand of the procedure.

This gradual information process must be reflected in each patient's clinical records; however, sometimes it's necessary to fill out a form called informed consent.  This form explains the risks involved in the intervention or diagnostic procedure as well as the individual risks and any possible side effects.  Please read this form carefully, and then sign it to give your consent.