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Supporting Pharmaceutical Customers to Achieve Compliance with Regulations for Track & Trace
CXV Global support pharmaceutical customers to achieve compliance with regulations for Track & Trace around the globe, including the EU Falsified Medicines Directive (FMD). Our Serialisation and Aggregation Software is specifically designed to meet the requirements of the pharmaceutical industry. We are the exclusive partner integrator for Antares Vision solutions for Serialisation, Aggregation and Track & Trace in Ireland, the UK, Benelux, Scandinavia and the US. The stand-alone Serialisation and Aggregation Modules ensure both efficiency and regulatory compliance. We design, integrate and support these systems in multi-site, multi-national projects for our customers.
As the Largest Partner Integrator Worldwide for Antares Vision, CXV Global have serialised in excess of 500 packaging lines over the last decade. Where regulations required aggregation to case or pallet level, we have advised and delivered on the equipment, software and integration to enable our customers to achieve compliance. Our serialisation project management teams collaborate with our customers to define and execute on a serialisation strategy that extends from packaging lines through the entire enterprise and supply chain.
These include Service Level Agreements, on-site and remote support, embedding engineers and IT experts within your teams, or entire serialisation Managed Service contracts. All of which are designed to eliminate disruption to your operations and ensure compliant batch production.
We’ve been leading the way in the solutions we bring to customer problems and in the deployment of leading edge technologies for over 30 years.
