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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Strategies to maximize outcomes for interactions during regulatory pre-submission meetings using 4 simple, but effective steps.
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FDA cybersecurity requirements for medical devices which are considered “cyber devices”, including US government definition.
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Overview of eSTAR, a joint Health Canada and FDA program streamlining medical device submissions with info on how to apply for the program.
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VR Design Tools – how does VR stack up to conventional methods in sketching and CAD? Discover areas in the design process where it excels.
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In silico medical device drop testing offers scalability, fast-tracking of iterations, and the ability to review hard-to-detect failure modes.
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Three concepts to improve teaming in medical device project management group are Handshakes, 5 Stages, and 6 Hats.
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Five tips to develop robust medical device commercialization strategies that engage a cross-functional team from engineering, production planning and supply chain.
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Medical device product definition tips ranging from general guidelines to regulatory, reimbursement, and hazard management.
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Engineering and QA/RA leaders share new technology, regulatory and supply chain developments that will impact future medical devices.
