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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Top 10 2015 StarFish Medical videos help connect viewers with employees they may only know from reading or phone calls.
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Top 2015 medical device blogs written by StarFish Medical expert employees sharing their knowledge, tips, and tools.
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Expedited Access Pathway (EAP) is promising for timely approval and access to devices for life-threatening or irreversibly debilitating conditions.
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Recent report on policies and initiatives claims the FDA device arm (CDRH) medical device approval process is much faster than five years ago.
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Sketch to Launch commercialization process for medical devices guides translational services to the medical industry.
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Advice, implications and examples for best time to implement a medical device Quality Management System in US, Canada and Europe.
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Meeting with the FDA can put almost everybody in the company in panic mode. Benefits of FDA meetings and what to expect.
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Medical device labeling includes all information provided with the device. Article identifies jurisdictions and associated "do's and don'ts".
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UDI compliance: What does that mean for your products and your company? Link to additional information about UDIs on the FDA website.
