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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Listening Strategy for Startups offers a three-pronged approach to stay competitive within the startup ecosystem.
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Outlines how medical device designers can perform in-house Medical Device Drop Test per IEC 60601-1 before third party testing.
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FDA Approved or Cleared Medical Device – the pathway you choose depends on the level of risk it represents and its intended use.
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RoHS 3 (EU 2015/863) expands the list of prohibited substances from 6 to 10 adding 4 phthalates. Learn if your device is RoHS 3 compliant.
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FDA ASCA Pilot Program is expected to bring medical devices to patients and users more efficiently by using ASCA-accredited labs.
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Medical device artificial intelligence (AI) overview of AI, applications and devices, investment landscape, and regulatory implications.
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2020 Medical device development videos include COVID implications for research and POC devices, optimizing founder value, manufacturing for NPI, IVD insights.
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COVID-19 Ventilator Design team discuss their top insights and lessons learned from the time constrained, critical ventilator project.
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How FDA Breakthrough Devices Program provides advantages for novel devices and can significantly reduce a product’s time to market.
