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HPRA Step by step guide - when to report an incident

Attached please find letter from the Human Products Monitoring Department of Health Products Regulatory Authority (HPRA). In the letter they outline specific activities that the HPRA is engaged in relating to the area of medical device vigilance which may be of interest to your organisation and its members.

Siobhán Foley (on behalf of Patrick Murphy, Medical Devices, Vigilance Manager)
Medical Device Vigilance Administrator
Health Products Regulatory Authority | An tÚdarás Rialála Táirgí Sláinte
Kevin O’Malley House, Earlsfort Centre, Earlsfort Terrace, Dublin 2.
Tel: +353 1 676 4971
Fax: +353 1 676 7836
devicesafety@hpra.ie
www.hpra.ie