PRISYM 360 Vision Inspection for Medical Device Labels
Medical Device manufacturers must adhere to very specific labeling requirements imposed by regulatory bodies, such as FDA UDI, EU MDR and similar regulations across a growing number of geographies. To distribute products in regions subject to governance by these bodies, product labels must be correct and compliant with specific regulations for that region.
Failure to ensure that all labels are clear, accurate and meet the necessary requirements creates risk of product recall, exposing organizations to the threat of heavy sanction from the regulatory bodies, whilst additionally leading to harm to patients or even loss of life.
Organizations need a solution that offers certainty to remove these risks. Find out how PRISYM 360 Vision Inspection solution can support your organization’s medical device labeling needs.