07th February 2020
Update on Plans for Ending Safety Features Use and Learn in Ireland on Phased Basis from 2nd March 2020
Following on from previous communications about plans to end the use and learn period on a phased basis, the Safety Features Oversight Group1 has now agreed that this will be done in the following phases starting from 2nd March 2020...READ MORE
01st October 2019
FMD Use and Learn Period in Ireland to End on Phased Basis from 31st January 2020
The National Safety Features Oversight Group comprising the Irish Medicines Verification Organisation (IMVO), the Department of Health, the Health Products Regulatory Authority (HPRA), the Pharmaceutical Society of Ireland (PSI), the Health Service Executive (HSE) and the Private Hospitals Association (PHA) continues to meet regularly to monitor...READ MORE
02nd September 2019
Announcement of extension to FMD ‘use and learn’ period in Ireland beyond September
New Falsified Medicines Directive (FMD) safety feature requirements came into effect on 9th February 2019. Since then the system in Ireland has been in a ‘use and learn’ phase to ensure the continuity of safe supply of medicines to patients while all parties gained a better understanding of the new system...READ MORE
24th June 2019
Announcement of new IMVO Head of IT
IMVO is delighted to announce the appointment of Dermot Byrne as Head of IT with IMVO. With experience built up over 25 years in commercial industry, across a range of roles, Dermot has managed both the technology and commercial aspects of business change and service delivery across the Irish, UK and US markets...READ MORE
08th May 2019
Decision to extend ‘use and learn’ phase
New FMD safety feature requirements came into effect on 9th February. During this time, the system in Ireland has been in ‘use and learn’ phase to ensure the continuity of safe supply of medicines to patients while all parties gained a better understanding of the new system. The national Safety Features Oversight Group comprising...READ MORE
08th February 2019
New medicines security features further protect supply chain for medicines
A new national and European system, giving patients further protection from the threat of counterfeit medicines comes into effect tomorrow (Saturday 9th February 2019). Throughout Europe, medicine packs will have enhanced tamper-proof measures and will now carry a barcode with a unique serial number so that each pack can be scanned...READ MORE
05th February 2019
Announcement of national approach to safety features implementation – initial ‘use and learn’ phase
Following discussions at a national level between the Department of Health, the Health Products Regulatory Authority (HPRA), the Pharmaceutical Society of Ireland (PSI), the HSE and Private Hospitals Association (PHA) stakeholder representatives and IMVO, it has been decided to adopt a pragmatic approach to the implementation of the...READ MORE
31st October 2018
Online registration for pharmacies and hospitals now open
IMVO is delighted to announce that online registration for pharmacies and hospitals is now open. This is an important milestone to assist pharmacies and hospitals in complying with new EU Falsified Medicines Directive (‘FMD’) requirements that come into effect on 9th February 2019. IMVO has contacted all community pharmacies...READ MORE
20th June 2018
First serialised pack decommissioned in Ireland
We are delighted to announce that the first serialised pack was decommissioned in Ireland in Moore’s Pharmacy in Crumlin, Dublin, on 20th June. We believe this may have been the first pack decommissioned in a community pharmacy anywhere in Europe using the ‘blueprint’ system model...READ MORE
30th May 2018
First serialised pack verified in Ireland
We are delighted to announce that the first serialised pack was verified in Ireland by PCO Manufacturing on 30th May, using their wholesaler connection to the Irish Medicines Verification System and the EasyFMD system supplied by Quick Pharm Solutions. Ireland was amongst the first five countries in Europe to start scanning...READ MORE
