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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Overview of Device Establishment Inspection Processes and Standards Update that establishes uniform processes and standards for FDA Inspection Process.
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Tips and a quiz for picking and approving calibration equipment vendors for medical device verification and validation.
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9 tips for 510(k) submission along with lessons learned from a recent successful experience submitting a medical device to the FDA.
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16 things to consider for the Medical Device Regulations (MDR Deadline) and changes you need to make in your Quality Management System.
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Why build a beta medical device? After a medical device receives regulatory clearance, it’s fairly burdensome to make changes. Beta device benefits are explained by experts.
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Insights and observations that spark medtech innovation are brainstormed by team of medical device professionals at StarFish Medical.
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Medical Device Playbook was conceived to inspire entrepreneurship and connect the many players. Here are commercialization Insights from attending the event.
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Closing the medtech skills gap: Who better to teach medtech skills within academia than those who are earning a living with those very skills?
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Medical device development experts share their biggest medical commercialization lessons learned over 20 years.
