Companies that have left it too late to implement their own solution will have to rely on support from providers, whose resources are already in high demand as the deadline approaches.
With only 3 months to go until the EU FMD comes into force, what can companies do now to ensure they are compliance ready? Experts from across the industry give their advice.
Brian Daleiden, Vice President of Industry Marketing, TraceLink
"The 9 November marks the 3-month countdown to the EU Falsified Medicines Directive (FMD) compliance deadline. EU FMD applies to all countries in the European Economic Area (EEA) with the exception of Italy and Greece, who have an additional 6 years to transition from their existing serialisation regulations to those of EU FMD. The EMVO (European Medicines Verification Organisation), which operates the central EU Hub to which manufacturers will report their serialisation data, and the NMVOs (National Medicines Verification Organisations), who receive that data against which products are verified, are working to the deadline.
"Marketing Authorisation Holders (MAHs) alone are accountable for on-boarding and connecting to the EMVO, therefore their serialisation solution must also provide for data exchange with trade partners such as contract manufacturers. The EU Hub has been live for some time, with a growing number of MAHs now fully operational to transmit their serialisation data.
"Of the 30 national systems that should be in place, there are three at risk of not being ready by February. For MAHs however, lack of national system readiness does not alter their legal obligation to serialise their products and connect to the EU Hub by the deadline. Even if the national system of a country to which they ship products is not yet operational, the product data must still be uploaded to the EU Hub once the national system is live.
"MAHs that fail to serialise their packs will be in breach of the law. If a pack is released after the deadline, it must bear safety features. The legal responsibility lies on the MAH: if an audit uncovers that a pharmacist has dispensed a pack that was manufactured after February 2019 without safety features, the repercussions will fall on the MAH, not the pharmacist. The pharmacist’s accountability is to verify and decommission all packs bearing safety features.
"The ultimate financial penalty is the rejection of your stock - if wholesalers and/or pharmacists can’t verify and decommission it, by law they can’t dispense it.
"With these implications in mind and with such limited time left, it is essential that businesses prioritise the on-boarding of partners, complete the EMVO On-boarding Partner Portal (OBP Portal) process and related NMVO agreements, connect to and verify integrations with the EU Hub, and validate their end-to-end EU compliance solutions.
"The on-boarding process, internal design of all technical and operational touchpoints needed for EU compliance, and connecting IT systems to the EU Hub across multiple data transactions can all be challenging; businesses that aren’t using a pre-validated solution have a lot of work to do in a very short timeframe. Businesses that have opted for point-to-point connections with contract manufacturing organisations (CMOs) and third-party logistics providers (3PLs) have created additional layers of complexity and are at risk of failing to meet the deadline.
"As companies make decisions that will dictate their readiness for the February 2019 FMD deadline, they will have to rely on support from providers that can deliver cost-effective, turnkey solutions. A network-tenant approach where a prevalidated solution connects manufacturers with their supply chain partners and enables the data exchange required for compliance is the only viable option for any business that isn’t already well underway in implementing a solution."
Erik Haeffler, Vice President of Manufacturing Services, Recipharm
"The deadline for serialization compliance is fast approaching. Three months is a very short period of time given the scale of the changes that are required to implement a suitable solution. Ideally, contract manufacturing organizations (CMOs) will now have finished testing and validating solutions to ...
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