Publication
EU Falsified Medicines Legislation - Update on National Arrangements for Implementation
From Department of Health
Published on
Last updated on
From Department of Health
Published on
Last updated on
On Saturday 9th February the European Commission’s Delegated Regulation (EU) 2016/161 on Safety Features on Medicinal Products for Human Use, comes into operation across Europe.
The Delegated Regulation supplements the Falsified Medicines Directive 2011/62/EU, by setting out detailed rules for the safety features appearing on the packaging of medicinal products for human use.
These new requirements will help to enhance patient safety by protecting the pharmaceutical supply chain from infiltration by falsified (or counterfeit) medicines and introducing new rules to more rigorously regulate the supply chain.
The Irish Medicines Verification Organisation (IMVO) has been established to manage the medicines verification system for Ireland and the vast majority of pharmacies, wholesalers, MAH’s and manufacturers have registered with the IMVO.
The Department of Health has been working closely with the IMVO, the Health Products Regulatory Authority (HPRA), the Pharmaceutical Society of Ireland (PSI), the HSE and Private Hospitals Association (PHA) for the last year to monitor progress in the implementation of the new safety feature requirements across all sectors.
This new medicines’ verification system is a significant undertaking involving the collaboration of almost 2,000 pharmacies and hospitals, along with pharmaceutical manufacturers and wholesalers, stakeholder representatives and regulators, which sees over 95 million prescription medicines dispensed to patients every year.
Notwithstanding the significant work undertaken to date and given the complexities associated with setting up the medicines verification system impacting all stakeholders in the medicines supply chain across Europe, it is anticipated that the initial period of operation will identify issues as the new system comes into effect Europe-wide.
Following discussions at a national and European level with stakeholder representatives, it has been decided to adopt a pragmatic approach to the implementation of the Delegated Regulation (and the associated statutory instrument) after the go live date, to ensure the continuity of safe supply of medicines to patients while all parties gain a better understanding of the new system. This means that:
National legislation including the provisions of Article 23 of the Delegated Regulation will be introduced, however, the offences provided for in the Regulations will not be commenced for a period of time to let the new system bed in.
During this period, the alerts generated will be analysed by the, IMVO, HPRA, PSI, HSE and the private hospitals pharmacies to determine why they are occurring and develop appropriate protocols for their resolution. Manufacturers (and marketing authorisation holders) will also be involved in the investigation of alerts generated against their products. The system will be reviewed again in three months’ time.
This approach will ensure that medicines continue to be provided to patients without delay and also ensure that all stakeholders, manufacturers, wholesalers, pharmacists and other healthcare professionals work to build confidence in operating the new safety system.
Additional Information
The Commission has published a Q&A document which addresses many of the key issues around implementation of the Delegated Regulation for Safety Features. The Department of Health advises all professionals expected to interact with the Regulation should read this document as well as the Commission’s dedicated Falsified Medicines webpage which provides additional relevant guidance.
Further background details are also available from the Falsified Medicines sections of the IMVO, HPRA, PSI websites and in the case of private and public hospitals from your assigned Project Lead for FMD.