Reporting Product Problems

This section of the IMB website provides mechanisms to report suspected issues via on-line forms to the Irish Medicines Board.

Adverse Reactions and/or Quality Defects associated with Human and Veterinary Medicines
Adverse Incidents associated with Medical Devices
Adverse Events associated with Clinical Trials
Adverse Reaction/Events associated with Tissues & Cells

All of the above may be reported through our on-line system or by downloading the forms through our publications section.

Please note that your on-line form will receive an acknowledgement at time of submission

To complete an online form relating to one of the above topics please select the link to the appropriate form on the left hand side of the screen.

The Irish Medicines Board - www.imb.ie

Reporting Product Problems