Resource Centre
Discover a wealth of knowledge and insights from the experts at StarFish Medical. Our Resource Centre offers product development tips, reviews of new and cutting-edge technologies, and in-depth articles on regulatory updates and compliance in medical device development.
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The Bleeding Edge explains how 510K cleared medical devices are clinically proven to improve patient outcomes and save lives.
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The book Bad Blood eloquently demonstrates the importance of properly developing medical devices under ISO 13485.
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Empathic Design paying attention to what female users say, think, do, and feel, gives a holistic understanding of user desires and needs.
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Alarm fatigue is influenced by a variety of factors. End user and patient behaviours are most identifiable through procedural observation.
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Setting up observation sessions can be quite time consuming. Three tips to make the most of your time and results.
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When observing a summative evaluation it is crucial that the observers do not influence the participants. Tips to avoid influencing results.
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Proper documentation is an up-front investment of time and effort that pays big dividends later in medical device development.
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FDA’s Early Feasibility Studies Program (EFS) is a great option in early stage development looking to advance your program by gathering data.
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Debunks three common unit testing myths and shares author’s experience using an automated tool when designing medical device firmware.
