Improving Compliance and Reducing Label Waste for an Implantable Device Manufacturer
A mid-sized surgical device manufacturer specializing in implantable medical devices faced growing challenges with its labeling process. As demand for its products increased, so did the complexity of labeling requirements, particularly with global expansion and evolving regulatory standards such as FDA UDI, EU MDR, and ISO 13485 compliance. Challenge The company relied on pre-printed labels sourced in bulk from an... View Article