Unclear labelling can lead to device misuse, regulatory non-compliance, and potential harm. At Eurofins Medical Device Services network of laboratories, we understand the science and the regulations, providing labelling that safeguards patients, supports professionals, and ensures compliance. Our graphic designers and Human Factors experts work closely with you to develop every aspect of your labeling, from the artwork for your device packaging and Instructions for Use (IFUs), to QSGs, to warning labels. We ensure your labelling is not just compliant, but effective. 

We apply human factors principles to develop clear, simple and easy to follow instructions that:

• Emphasizes critical steps and warnings
• Color codes essential information
• Logical layout and user-friendly formatting
• Understood by the target users
• Uses clear, consistent phrasing and terminology
• Visual aids to address/reduce cognitive load

Coupled with our labeling comprehension studies for regulatory submissions, we ensure users fully understand a device, its risks, and safe use when labelling is read and followed.

Ensure your labelling is clear, compliant, and user-ready.