Mado Systemy supports LEK-AM with serialisation
Target successfully reached We would like to briefly describe how the combined teams of MADO SYSTEMY and LEK-AM companies developed as a project team. Goal was a comprehensive implementation of serialisation of medical products in accordance with the requirements of the EU Falsified Medicines Directive (FMD). We’ve covered a four production lines in a modern […]
In search of operating efficiency post Serialization
Just over a year ago since the implementation of the European order against drugs counterfeiting, the industry is still struggling with productivity levels.
Achieving global UDI compliance with WIPOTEC-OCS
As in the case of serialization regulations in the pharmaceutical industry, UDI compliance for medical device manufacturers is soon to become a global matter. Following the EU UDI regulations for medical devices and in vitro diagnostic devices, more countries have already issued guidance or a draft of their own localized UDI requirements. Here are just […]
Serialization and aggregation in Russia from 2020
Mado Systemy together with WIPOTEC-OCS is ready for the scenario with a large signature containing 88 characters.
Serialization in Small and Medium Pharma Company
Serialization in Small and Medium Pharma Comapny: How to get ready for European FMD from the software point of view?