2016 is a landmark year for patients across Europe. The implementation of the Falsified Medicines Directive starts the journey towards safer medicines for all who need them. This process begins with the publication of the Delegated Regulation and ends will all member states protecting their citizens with a secure, fast and reliable medicine authentication service. Aegate welcomes this significant improvement and looks forward to working with all stakeholders to make it happen.'
With the publication of the Delegated Regulation on February 9 2016 the time available to implement the Falsified Medicines Directive reduces every day. That is less time to connect 170,000 pharmacies, less time to test, less time to be ready to scan 10 billion packs every year and less time to protect the 500 million citizens of Europe.
The Aegate Demonstrator program.
As 2D bar codes begin to enter the European market, manufacturers must find a way to prove they are fit for purpose. Test your codes in a proven authentication service. Talk to Aegate about our Demonstrator Program today. From upload to dispense, Aegate will help you to be ready for the FMD deadline.
The Aegate NMVO Stakeholder Guide – are you asking the right questions?
Our expert advice for stakeholders forming their local NMVO can be found here.
Ensure your country’s Authentication Service is the best in can be in terms of security, compliance, operation and governance.