The Irish Health Products Regulatory Authority publishes guidance for distributors of medical devices

A guide for distributors of medical devices has been published by the Irish Health Products Regulatory Authority (HPRA). The document provides distributors with supplementary guidance and recommendations for best practice in Ireland. The obligations for distribution of medical devices are covered, including in vitro diagnostic medical device distributors in the IVD and MD Regulations.

Please click here to read the full document.

Tagged with

Published on 6. March 2018 in News Ireland