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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One of the key requirements for ISO 60601-1 is the protection against water ingress in Medical Devices. Three areas to watch are discussed in this article..
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There are a lot of things to consider when creating a summative usability test. The first time can be overwhelming. What scenarios do I test? How do I identify a critical task? How many participants do I need? Do I need to test the training? In this eGuide I will help you avoid common mistakes, like using a formative test structure for a summative usability test. I will also provide some tricks and tips to help you get the most out of your test participants and testing.
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Chimeric antigen receptor T-cell (CAR-T) therapy is a rising shining star in Regenerative Medicine. Medical devices will be involved.
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Watch the most viewed StarFish Medical videos of 2018 to learn about medical device design, development, regulations, and manufacture.
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The book Bad Blood eloquently demonstrates the importance of properly developing medical devices under ISO 13485.
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Five eye diseases that account for the majority of issues related to blindness or poor vision. Diagnostics and treatment of these diseases are often performed with precision opto-mechanical medical devices that continue to increase in reliability and accuracy and decrease in price every year.
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Open Source Software Medical Devices: Using OSS libraries within a Software System of a Medical Device or In Vitro Diagnostic Device.
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When selecting a method for developing an assay, whether it is for detecting bacteria or simulating fluid, the approach all depends on…
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Assay industry trends overview includes infectious diseases diagnostics industry continuing to expand into traditional diagnostic areas.
