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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Insufficient testing and premature optimization can lead to a rush to the wrong medical device in the product definition phase.
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Embed error detection and correction in the message itself to avoid communication errors in medical device development.
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10 questions a medical device company needs to ask to determine if a small manufacturing services provider is the right choice for them..
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Feature additions need to be managed carefully to avoid scope creep overruns in cost or schedule, or jeopardize a 60601 submission or FDA audit.
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Project managers must be vigilant preventing scope creep in software & firmware design, from architecture definition to the production floor.
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Article with update links on 2012 US Medical Device Tax in the US and blogs with controversial views of the tax impact on the industry.
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What Makes You Unique? Your medical device design, product development, and manufacturing firm's answer should win your business.
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A wonderfully powerful and talented medical device design team can be undermined by omitting a critical expertise – the Tooling Engineer.
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Why is the ISO 8601 standard not used for the date format (i.e. 2012/07/02) for FDA UDI instead of the proposed format (i.e. Jul 02, 2012)?