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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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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Medical Device 510(k) and CE Marking similarities and differences to help companies effectively prioritize their regulatory efforts.
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Highlights of July and August 2014 medical device FDA guidance documents that reduce regulatory burden without compromising patient safety.
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Tips, considerations, and techniques to increase IVD Regulatory Success that is essential for many Medical Devices.
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MDSAP enables Medical Device companies to save in Registrar’s fees, eliminate duplication of inspections and gain faster access to markets.
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Reduce costs by reusing IVD Verification Test equipment for verification of optical components as part of manufacturing quality control.
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Regulatory affairs expert explains how to write a best practice ISO 9000 Medical Device Quality Manual using 3 simple rules.
