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Medtec Ireland 2017 Conference: How Documentation Supports Usability

The program for the upcoming Medtec Ireland 2017 Conference (Galway, 4–5 October) reflects the increasing focus on the end user in the medtech industry. The Food and Drug Administration (FDA) and international regulatory bodies have recently issued various appeals to pay more attention to usability. This has strengthened awareness in the medtech community of the […]

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Untap the Value of Medical Technology Documentation

Every stage of the medical technology product lifecycle demands detailed documentation. Does it have to be a headache? This post was originally published in September 2016 and updated in September 2017. Unfortunately, the very mention of the term ‘documentation’ can induce instantaneous migraines in Risk and Compliance Officers, Regulatory Affairs Managers, Quality Controllers, and Process Engineers, […]

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