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 of 2024 Regulatory trends include QMSR, LDTs, FDA guidances, and timelines in the EU for MDR and IVDR.
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FDA Real-World Evidence Draft Guidance analysis identifies five key points to help understand the potential impact of the draft guidance.
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How a ready-made modular proof of concept system for rapid prototyping Point of Care Diagnostics can expedite and de-risk product development.
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The modular platform for transferring immunoassays acts as an intermediate bridge and is a significant step towards streamlining the product development process for diagnostics.
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Medical device software is very diverse. In all this variety, one technology is ubiquitous: Git! Three eye-openers which help developers use Git better.
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Inventory Risk Management is an important factor for long-term growth and competitiveness in the medical device industry. Learn five key areas to watch.
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2023 top 10 medical device commercialization videos cover a variety of medical device commercialization topics ranging from Prototyping Proof of Concepts to Writing Medical Device Manufacturing SOPs.
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The top 10 Medtech Entrepreneur Webinars of 2023 feature medtech executives, serial entrepreneurs and experts discussing topics for medical device entrepreneurs.
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Successful medical device exits for startups often involve a combination of other important business factors. These 18 factors are the most important to a successful exit.
