On 5 June, the European Commission published a Commission Notice providing further clarity about the Packaging and Packaging Waste Regulation in practice. We take a closer look at the document to understand its requirements in detail, including the current status of PFAS restrictions, the…
In this Innovation Spotlight, Dow outlines how its extrusion coating portfolio aims to support recyclability requirements and regulatory readiness, and how its collaboration with RDM Group demonstrates how lightweight polymer coatings can extend the use of fibre-based packaging into applications…
TraceLink Inc. has unveiled an industry first: an integrated Compliance and Digital Information Platform for pharmacies with EU Falsified Medicines Directive (FMD) requirements.
The anti-counterfeit market is expected to double its 2016 revenue figure by 2021 however; packaging and labelling professionals are presented with several challenges to overcome before they can make this a reality.
Ahead of Nexus 17, keynote speaker and Tjoapack founder Eric Tjoa recalls the journey towards the EU FMD and shares his predictions for the future use of technology as the pharmaceutical sector commits to protecting patient safety.
Systech International, a global technology solutions leader for the pharmaceutical industry, has announced its upcoming serialisation webinar titled "The Clock is Ticking: Overcoming the Challenges of Implementing Serialisation in the EU".
New industry research reveals that more than one third (36 per cent) of pharmaceutical manufacturers and contract packagers are not currently preparing for global serialisation requirements, despite impending deadlines.
TraceLink Inc., the world’s largest track and trace network for connecting the life sciences supply chain and eliminating counterfeit prescription drugs from the global marketplace, has announced the latest keynote speakers confirmed for NEXUS 17
