Dear Medical Device Stakeholder,
Your industry representative body has kindly agreed to distribute the attached letter (attachment I) on behalf of HPRA.
The purpose of the letter is to inform stakeholders of the new fees that will be implemented from 1 January 2017 and to request contact information so that HPRA can contact organisations directly on the matter of fees.
We could be grateful if you could respond to devicefee@HPRA.ie with the necessary contact details or go to the following website:
Human Products Authorisation & Registration Dept
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