As a result of the EU FMD Regulation, diverse Alerts are created due to the detection of falsified packs or due to procedural or technical errors. The management of these Alerts in high numbers is a significant challenge.
In order to meet the various requirements of all involved stakeholders like National Organizations, Pharmazeutical Industry, National Authorities and End Users we developed two Product Lines of NMVS Alerts.
Both Product Lines cover the specific requirements and offer the necessary functionality scope for an efficient resolution process.