Accurate and compliant labeling is crucial for the safe and effective use of medical devices. At confinis, we assist clients in developing and implementing labeling strategies that meet regulatory requirements, including Unique Device Identification (UDI) requirements. Our services include creating and reviewing labeling content, ensuring accuracy, and verifying compliance with relevant standards.

We help clients navigate the complexities of UDI implementation, including data submission to regulatory databases and integration into existing quality systems. Our expertise in labeling and UDI ensures that clients’ products are properly identified and traceable, enhancing patient safety and regulatory compliance.