With a focused approach, Domino has become the preferred strategic provider of coding and marking solutions to numerous manufacturers and OEMs.
The innovative coding and marking systems are designed to meet the GMP (good manufacturing practice) validation requirements, alongside implementing global legislation standards such as the EU regulation 2016/161 to execute the Falsified Medicines Directive 2011/62/EU, the EU Medical Device Regulation 2017/745, 21 CFR Part 11, e-Pedigree, SFDA, ANVISA and the US FDA UDI.
Domino also provides trusted solutions for aggregation, i.e. the establishment of connected data at each stage of the packaging process.