Medical Devices Labeling Requirement for EU MDR Compliance
As the EU MDR transition deadline is inching closer, manufacturers must execute the labeling requirements with utmost priority and caution and must ensure high standards of quality, and safety for compliance. Prior to execution, understanding the new labeling requirements and accurate implementation is of paramount importance. Any labeling errors can impede the progress, cause product recalls and lead to costly delays.
Therefore, the key is to carefully prepare the medical devices labels aligning with the EU MDR labeling requirements, such as: