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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Differences noticed between design in school and in real world medical device design during my internship at StarFish Medical.
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Medical device sketching is an effective tool to help clients visualize how their ideas might look like as a fully realized product.
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Procedural observations of medical procedures are invaluable and inform designs with perspective of users, procedural workflow and intended use environment.
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3 Medical UX design differences between the graphical user interfaces (GUI) of digital displays in medical devices and consumer products.
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How to handle recent medical product development regulatory changes under the 21st Century Cures Act and device exemption list.
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Start early to avoid surprises when preparing for MDR 2017/745. The new EU medical device regulations will come into full force in Q2 2020.
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Tips to manage competence and training, keep up to date and ensure personnel are trained and competent to perform their duties.
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MDSAP Medical Device Single Audit Program audits will help ensure compliance with QMS and reduce the audit/inspection burden.
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How to prototype medical device parts in 4 steps by using SLS printing to replace traditional sheet metal prototype parts.