As long as a product’s packaging and labelling is treated separately from internal regulatory and product information management, the scope for inefficiency, error and risk remains significant — especially with the growing frequency of regulatory updates around the world. With this in mind, AMPLEXOR’s Romuald Braun explores the potential to make label management a less superficial activity.
Beyond surface value
Mislabelling is one of the leading causes of costly product recall,1 and a particularly frustrating one given that it is so easily preventable. Yet, as long as product labelling is treated as a distinct, manually-driven process, life sciences organisations will continue to leave themselves open to the risk, not to mention a level of inefficiency they can ill afford.