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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Ariana and Mark explore how prototype strategy helps teams reduce technical risk and accelerate progress.
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In the world of medical device development, requirements are often treated as a regulatory tax, essentially documentation created solely to satisfy a compliance need.
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After years of working with founders and technical teams, I have learned that early design missteps rarely come from engineering flaws. More often than not, they come from missing conversations.
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Ariana Wilson and Mark Drlik explore how teams can reduce the device development timeline without compromising quality or compliance.
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Bringing up a new printed circuit board assembly (PCBA) for a medical device is both exciting and high-stakes.
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Several design considerations come into play when designing portable medical electronic devices, from performance, to usability, manufacturability and reliability.
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For many medical devices, power stability isn’t just a nice-to-have, it’s mission-critical.
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A structured, well-documented design review process is a critical component of successful product development, particularly in the medical device industry.
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I routinely engage in the development of prototype medical devices. These prototypes typically incorporate at least one printed circuit board (PCB) installed within a plastic or metal enclosure, featuring numerous connections to external components through various connectors.
