Manufacturers and parallel distributers are required to change their packaging to include an anti-tamper proof device, additional human readable information and include a 2-D barcode. In addition, they are required to upload the data into a Europe-wide database for verification and de-commissioning of medicine packs by end users.
Access to the European FMD database is controlled via the National Medicine Verification System (NMVS). Mysoft is a registered software supplier and has created an interface to allow verification and de-commissioning of medicine packs. The interface has successfully been deployed at a major pharmaceutical business in the UK.
Mysoft will also provide additional services to help integrate the FMD pack into your business processes. We can also provide expertise to help set-up scanners to read 2-D barcodes.
Find out more about our expertise in the Pharmaceutical Industry, click here.