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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FDA medical device accessory guidance lessens regulatory burden, permitting low risk devices to market faster and cheaper.
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Overview analysis of the FDA’s 2019 guidance on low-risk devices for general wellness and medical device accessories.
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StarFish Medical device development videos viewing is up 38% in 2014. Countdown of the Top 10 most viewed videos in 2014.
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Most read StarFish Medical Device Development Blogs of 2014: regulatory information, analysis, testing, design, career path, and finances.
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Staffing a Medical Device Start-Up: shortlist of job descriptions required to develop a complex, novel medical device.
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Medical Device 510(k) and CE Marking similarities and differences to help companies effectively prioritize their regulatory efforts.
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FDA MDDS and mobile medical applications guidances; what they mean & where they apply. Article identifies common sense approach by FDA.
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Milestones and insights on taking a medical device idea from concept through to manufacture. Identifies a few false ‘done’s along the way.
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Analysis of IEC60601-1-2 (2014) 4th Edition update. Includes examples and impact on medical device regulatory testing and commercialization.
