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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Areas to be considered in Summative / Human Factors Validation planning, include test environment, and user profile review.
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Translating user and patient insight into tangible design offers tips and techniques for industrial designers and human factors researchers.
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PM, EE, ME and ID/HF Manager insights and examples of how Medical Device Human Factors and ID impact Commercialization success.
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Formative Evaluations and Tests details the differences between these two methods, and the appropriate circumstances for their application.