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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Will consumer electronics engulf the medical device development community, making rigorous testing and risk mitigation processes obsolete?
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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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Results of StarFish client satisfaction survey with a large group that included customers and prospects using one word descriptions.
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Regulatory affairs expert explains how to write a best practice ISO 9000 Medical Device Quality Manual using 3 simple rules.
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Highlights from Day 1 of Learning Lab event at Boston BIOMEDevice on electro-medical device basic safety and achieving compliance with 60601.
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Six ways to manage and communicate medical device project relationships without losing the essence of the development innovation or wasting money.
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Medical Device Pathfinder process for Intellectual Property, Consumables Strategy, Value Chain and Margin, and Reimbursement.
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Medical Device Design and Development Process Improvement for Annual Plan: limit improvement efforts, measure them regularly, succeed.