Adverse event reporting

  • Kowa routinely monitors the safety of their medical devices supplied to the European market. This includes review of safety data from clinical studies and the collection of Vigilance issues for marketed devices.

  • Patients and volunteers in clinical studies that experience an adverse event should contact the investigator.

  • Patients receiving a marketed device should contact their doctor or the clinic concerned to report any issues.

  • Alternatively, within the EU adverse events may be reported to:

    Kowa Medical Care Europe GmbH
    Heinrich-Heine-Allee 22
    40213 Düsseldorf,
    Germany

  • E-Mail: info@kowa-deutschland.de