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Understanding updates on medical device labelling

May 11, 2023

Medical device labels aim to inform patients and healthcare providers on how to use and maintain instruments, as well as communicating safety or associated risks.

As device and diagnostic manufacturers worldwide develop new products to improve patients’ quality of life, labels and instructions-for-use (IFUs) are essential in developing trust between healthcare practitioners and supporting consumer confidence.

Quality and compliance are continual priorities in medical device labelling as the industry looks to adopt new procedures and systems to ensure standardisation, consistency, and reliability.

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