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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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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Biological sciences medical device breakthroughs for this decade have a solid base to build upon. Here are our top five picks for the 2020's.
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Dr. Katherine Elvira speaks about her work developing lab-on-a-chip (microfluidic) technologies to investigate how drugs enter human cells.
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Developing a “lab-on-a-chip” (LOC) solution brings unique challenges and benefits. 6 tips for developing a “lab-on-a-chip” (LOC) solution.
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The amount of total company funding to develop a Class II 510(k) cleared medical device is approximately $30 million. The development and engineering costs comprise approximately $2-5 million of this total. This estimate is built upon a meta-analysis of various references as well as our experiences in engaging with companies. Many factors influence these costs, including the need for clinical studies, regulatory pathway, and technology complexity. Refinement of these numbers requires a professional team to understand the technology, regulatory, and business opportunities.
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Testing Medical Devices in a Biolab? Pre-planning is required for specialized tests, potentially dangerous microorganisms, tissues and biological fluids.
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How to create accurate and functional 3D models from patient imaging data. Develop anatomically accurate prototypes for medical device design.
