The European Union’s Medical Devices Regulation (MDR), published in May 2017, marked a significant shift in how medical technologies are tracked, verified, and brought to market within the EU. With sweeping changes affecting manufacturers, importers, distributors, and notified bodies, the regulation’s provisions on Unique Device Identification (UDI) drew particular attention from supply chain and compliance […]
The U.S. Trade Facilitation and Trade Enforcement Act (TFTEA), enacted in February 2016, marked a turning point in modern customs oversight and trade data transparency. By 2017, importers and supply chain managers began to feel the practical effects of its provisions, particularly those tied to Section 301. This section, initially designed to strengthen the enforcement […]
The amendments to Canada’s Access to Cannabis for Medical Purposes Regulations (ACMPR) in May 2016 marked a significant tightening of regulatory expectations across the country’s medical cannabis sector. By 2017, the impact of these amendments could be felt in every part of the supply chain, from cultivation sites to patient sales points. The central requirement […]
The 2023 updates to Japan’s Act on Promotion of Resource Recycling marked, in many respects, a turning point in the country’s approach to tracking e-waste. While the original 2020 legislation already laid down a framework for promoting circularity in materials use, the latest revisions take a more assertive stance on traceability, particularly when it comes […]