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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Understanding medical device classifications is critical for compliance, risk management, and time-to-market success. Whether you’re designing a wearable sensor or a life-sustaining implant, knowing how your device fits into FDA Class 1, 2, or 3 categories is essential.
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Delivering a drug to the right place at the right time can define the success of a therapy. Yet understanding delivery routes, devices, and technologies across the body can be complex.
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This in-depth drug delivery strategy guide from StarFish Medical explores how to design, develop, and deliver breakthrough drug-device combination products.
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Choosing the right design and development partner is one of the most critical decisions in bringing a medical device to market.
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AI is quietly reshaping how hardware teams work. At StarFish, it’s become a versatile collaborator across the product lifecycle from early sketches to prototype validation.
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User Experience (UX), Human Factors (HF), and Industrial Design (ID) each have a major impact on the success of new medical devices. Their influence is especially important during product definition and early phases of device development.
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Medical device startups/founders and enterprise partners have unique strengths and goals, which are often reflected in the way they work with CDMO (Contract Development and Manufacturing Organizations) partners.
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A structured, well-documented design review process is a critical component of successful product development, particularly in the medical device industry.
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You have a great MedTech innovation idea and are trying to decide whether to build a team to commercialize a medical device…
