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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Nick and Joris tackle a topic that’s more relevant than ever—raising funds for medical device development in today’s challenging financial landscape. With economic headwinds and cautious investors, startups and even established organizations face significant hurdles in securing funding. But there are ways to mitigate these challenges, and Joris shares strategic insights to align product development milestones with fundraising cycles.
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In this episode of Bio Break, Joris van der Heijden and Nick Allan discuss the critical role of specialized facilities in the successful development of medical devices. From testing laboratories to clean rooms, they explore the infrastructure needed to support innovation and ensure safe, effective products reach the market.
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Whether you’re in the early stages of a new project or refining a product concept, this episode of Bio Break delves into the foundational importance of a well-defined Target Product Profile (TPP) in medical device development. It’s packed with practical advice and expert insights to set you on the path to success.
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Inventory Risk Management is an important factor for long-term growth and competitiveness in the medical device industry. Learn five key areas to watch.
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The top 10 Medtech Entrepreneur Webinars of 2023 feature medtech executives, serial entrepreneurs and experts discussing topics for medical device entrepreneurs.
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Successful medical device exits for startups often involve a combination of other important business factors. These 18 factors are the most important to a successful exit.
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A medical device commercialization vision helps develop a road map to identify the best path to achieve milestones.
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33 tips and examples from commercialization experts for manufacturing a medical device.
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Review of the FDA Selecting a Predicate Device to Support a 510(k) Submission Draft Guidance on Best Practices