Registration of persons responsible for placing In-vitro Diagnostic Medical Devices on the market in accordance with Directive 98/79/EC and S.I. No. 304 of 2001

The application for the registration of people and/or companies accountable for placing in-vitro diagnostic medical devices on the market has been changed by the Irish Medicines Board. Part of the change includes an update for applicants on the instructions of how to submit this application to the Irish Medicines Board.

Please find the application here.

Source - http://www.imb.ie/EN/Publications/Publications/Registration-of-persons-responsible-for-placing-Invitro-Diagnostic-Medical-Devices-on-the-market-in-accordance-with-Directive-9879EC-and-SI-No-304 of-2001.aspx?page=7&year=0&categoryid=&letter=&q