Anne Hayes has worked with the Irish regulator, the Health Products Regulatory Authority, for over 21 years. She has been in the role of Inspection Manager for 15 of those years and has responsibility for inspection programmes relating to Good Manufacturing Practice, medical device auditing, Good Clinical Practice, Good Pharmacovigilance Practice and Good Practice in relation to blood, tissues and cells and organs for transplantation.
In January 2020 Anne became the PIC/S Chairperson.
Before joining the HPRA, Anne worked in the pharmaceutical industry for 5 years as a QC Supervisor and as a Qualified Person (QP).