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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Review of the FDA transition plan for medical devices currently marketed under Emergency Use Authorizations with implications for devices.
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How the FDA Catalog of Regulatory Science Tools can reduce risk in medical devices and explores several tools and categories.
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Medical Device New Product Introduction (NPI) & Commercialization lessons for medical device strategy, design, development, and NPI success.
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Outlines how medical device designers can perform in-house Medical Device Drop Test per IEC 60601-1 before third party testing.
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Considerations when developing a diagnostic product that is intended for use outside a traditional laboratory.
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Microfluidic Optics explores ways that lenses can be implemented on microfluidic cartridges can play an important role in microfluidic platforms,
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Designing Microfluidic Cartridges offers five critical considerations to increase success during microfluidic cartridge development.
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Five examples of Microfluidic Machine Learning enabling microfluidic technologies to push into new areas and applications.
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The intent of this checklist is to aid self-assessment of your medical device commercialization readiness relating to regulatory requirements. Compare the answers you provide with stages from the StarFish Product Development Process at the end of the checklist to identify how ready you are for applicable regulatory requirements.
