Pharmaceutical Serialisation
With the Falsified Medicine Directive (FMD) now in effect, Alloga is fully compliant with the regulatory requirements
FMD Compliance
Counterfeit medicines can be enormously problematic for the pharmaceutical industry, leading to the loss of patient confidence as well as to a loss of revenue. The European Falsified Medicines Directive (FMD) went live on 9 February 2019, with the aim of reducing the number of falsified medicines entering the European medicines supply chain.
Verification & Decommissioning
According to the EU FMD, products must be verified and decommissioned by a hospital or pharmacy before being dispensed to the patient. Alloga can verify and decommission products on behalf of manufacturers for Article 23 customers. Institutions covered by Article 23 depending on the EU country include veterinarians, paramedics and emergency medical practitioners, hospices, prisons and nursing homes, amongst others.
Related Technology
Alloga’s market leading technology supports robust and flexible integrations with internal logistics management systems. Learn more about our platforms and integration services here.
Alloga Gateway
The Alloga Gateway offers near real time data for all stock stored within Alloga system at any given point.
Technical Integration Service
Alloga’s Technical Integration Service enables easy integration between our system and those of our clients
Speak to a Specialist
Get in touch with our international logistics network experts to find out how Alloga can help you build efficient and reliable supply chain solutions.