G-NO TERAPIA
Contraindications

As a producer of medical devices, ALTERUM MEDICA is obliged to introduce
a vigilance system to report any adverse events occurring in the use of its
medical devices to the relevant healthcare authorities.

The purpose of the vigilance system is to ensure the health and safety of patients
and other persons using the medical devices by reducing the reoccurrence
of the same type of adverse events. It is achieved by the immediate reporting
of such events which allows for corrective and preventive steps.

Users of the ALTERUM MEDICA products who experience any adverse event regarding
the product is obliged to report it immediately to ALTERUM MEDICA or any
local ALTERUM MEDICA Sales Representative.

Notifications can be sent by e-mail, fax or phone.

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