Solidsoft Reply has released VeriLite 2.3.4. Our latest update is filled with improvements designed to make reporting simpler and enhance user experience in our lightweight, FMD compliant, cloud-based verification solution.
Deployed in late March 2024, VeriLite 2.3.4 is available to all countries and markets, required by law to use the European Medicines Verification System (EMVS) for pack identifier verification. This latest release further extends support to wholesalers, pharmacists, and doctors across Europe, including our customers in Bulgaria, Cyprus, Denmark, Finland, Iceland, Ireland, Sweden, and Poland. As a reliable and Falsified Medicines Directive (FMD) compliant tool, VeriLite ensures the accurate verification and reporting of medicinal packs bearing unique identifiers. By leveraging the solution, users can make requests to national systems, minimising the risk of falsified medicines entering the supply chain.
You can now enjoy the following VeriLite enhancements:
Pharmacists and wholesalers across Europe are required by law to use the European Medicines Verification System (EMVS) for pack identifier verification. Our VeriLite solution aligns with the EMVS' 'system of systems' approach and contributes to the overall advancement of the pharmaceutical landscape in Europe.
For more information, visit VeriLite or contact us here.
Solidsoft Reply is a leading technology company creating award-winning solutions utilising the Microsoft Azure cloud platform. As a globally acclaimed Microsoft AI Cloud Solutions Partner, we specialise in GS1 traceability systems worldwide, crucially ensuring the authenticity, legality, and safety of our customers’ products and services. Serving non-profits, NGOs, healthcare, and the pharmaceutical industries, we deliver technology for positive social impact. Your products, safe in our hands.