
The platform supports pharmacies, hospitals, distributors and parallel importers by enabling full traceability, product authentication and compliance with international regulations such as the EU Falsified Medicines Directive. Every medicine pack receives verifiable identification, allowing organisations to validate origin, batch, expiry date and authenticity before dispensing.
A fully certified solution developed in accordance with EU regulations for the Falsified Medicines Directive and all related safety-feature requirements. The platform adheres to official European standards for serialization, verification and decommissioning, ensuring seamless integration with the EU Hub and national systems.
For companies introducing new products to the market, we provide full support with serialisation setup and EU Hub registration, ensuring each item complies with regulatory standards from day one. Parallel importers gain a reliable system for re-serialising and tracking imported medicines, creating full traceability and compliance across borders.
Medicine authentication and verification
Real-time serial number scanning
Automatic FMD compliance checks
Pack status updates and decommissioning
Inventory protection from falsified products
Secure audit trail for all transactions
Integration with pharmacy and hospital management systems
Full product serialisation for new batches
EU Hub registration and data upload
Compliance with EU Falsified Medicines Directive
Pack aggregation, re-labelling and re-serialisation
Tracibility tools for parallel-import operations
Batch and logistics data management
Secure reporting and regulatory documentation
calibri.lv calibri.lv