We recently shared how Unique Device Identification (UDI) systems are an integral part of streamlining regulatory processes. There are also numerous articles touting the benefits of cloud-based labeling solutions further supporting the importance of medical device labeling. What we don’t often hear about are the personal stories of how these regulatory processes and labeling solutions impact the final users of the products.

Our Loftware partners share a personal story of the importance of the medical device regulatory process, as well as medical device labeling, and how one of them saw firsthand the reassurance they felt knowing the proper steps were taken to ensure the devices were safe, and labeled correctly. When faced with a medical emergency, it is not the time to question whether the device or medical equipment has met the regulatory rigors. This patient was much closer to these products than most, having been an integral part of working with the client who produced the products and played a role in ensuring the labeling of the products was accurate.

Unique Device Identification (UDI) systems “have been implemented globally” they improve patient safety, enhance the traceability of medical devices, and streamline regulatory processes. The project team at Pragmatyxs works closely with all our labeling partners to stay up to date on their labeling solutions and updates on regulatory compliance. Staying informed of technological advances in both the medical device industry and the labeling field allows us to continue offering our customers the best solution for their needs. Loftware also takes this opportunity to leverage advanced labeling solutions, so they too, can ensure more people “receive the right care at the right time, ultimately saving lives.”