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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6 benefits mean the FDA program for breakthrough medical devices may be your best regulatory option for novel medical devices.
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FDA's Early Feasibility Studies Program (EFS) is a great option in early stage development looking to advance your program by gathering data.
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Proper research and communication with authorities in each country of interest will make Medical Device International Regulations smoother to navigate.
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Dr. Joe Burkett, an emergency medicine physician shares his Medtech entrepreneur journey as Founder & CEO of Vaid Medical Devices.
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Kepner-Tregoe’s original Decision Matrix overview with tweaks to make it broader and more robust.
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Five things project managers can do to achieve great results and empower team members to perform at their best.
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Managing evolving requirements is a core competency for medical device technical specifications and understanding health care end users.
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11 medical device development mistakes that surfaced frequently in a variety of products. Avoid them to reduce cost and time to market.
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Assay industry trends overview includes infectious diseases diagnostics industry continuing to expand into traditional diagnostic areas.
