If you experience any adverse reaction or incident because of using a medical device owned by Euro-Pharma S.r.l, please contact your doctor or pharmacist. Please also report such reactions in the following ways:
- The health care provider must submit the incident report to the Ministry of Health by filling out the online form: Incident report by health professionals to the Ministry of Health. The form generated is automatically forwarded to the Dispovigilance system of the national device-vigilance network according to the provisions of the Decree of the Minister of Health of 31 March 2022. For more details, please consult the Circular of 29 November 2022.
- In the event of a complaint, the health professional is required to make a report to the manufacturer. He can also send the report to the Ministry of Health at the e-mail address
This email address is being protected from spambots. You need JavaScript enabled to view it. using the form attached to the Circular of 29 November 2022, to which please refer for more details. - Contacting Euro-Pharma S.r.l at: +39 3461524287 or by filling in and sending the following form:

