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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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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Biotech in medical device companies: 3 compelling reasons to pursue a Bio Services career in medical devices.
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Tolerancing is the consideration of process accuracy (and, to some extent, precision) when designing a device or component.
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Case studies show value of qualitative research in medical device design, illustrate human behavior is not calculable or quantitative.
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How to avoid typical manufacturing pitfalls using basic principles from the Office of Human Research Protections, Edward Deming, and others.
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LEAN Manufacturing Techniques for Medical Device NPI that will help ease medical device NPI transfers and generate value.
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Overview of Supply Chain Reports essential to assess and monitor costs, processing and material flow in medical device manufacturing.
