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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  • Aerosol Drug Delivery Systems graphic

    Aerosol Drug Delivery Systems, including Aerosol-based pulmonary-delivered drug devices, offer significant value by enabling targeted drug delivery directly to the respiratory system.

  • A medical vial with liquid and several teal-and-white capsules floating in the air, with a text overlay reading "Drug & Device: Why combine?" in a lab setting background.

    In this episode of Bio Break, Joris and Nick explore the increasingly important world of drug-device combination products, discussing what they are, why they matter, and the unique challenges associated with their development. As modern pharmaceuticals become more complex, the role of engineered medical devices in delivering these therapies safely and effectively has never been more critical.

  • An illustrated flow diagram with interconnected boxes, representing platform technologies in a modern office setting. The title 'Platform Technologies Pros & Cons' is displayed prominently in bold purple and green text, suggesting an exploration of benefits and challenges in the field.

    In this engaging episode of Bio Break, Nick and Joris dive into the complex world of platform technologies in product development, exploring the pros and cons of this widely discussed concept. From in-vitro diagnostics to point-of-care instruments, the term “platform” often sparks excitement—and sometimes hesitation. But what does it truly mean to build a platform-based product, and when does it make sense?

  • Colorful candy-coated chocolates float in the air against a blurred indoor background. Bold purple and black text on the left reads: "Medical Device Safety – A lesson from Van Halen."

    Nick and Joris dive into the surprising connection between rock bands and medical device safety. What do jelly beans and 1980s rock legends Van Halen have to do with developing safe and effective medical technologies? More than you might think.

  • Abstract image depicting financial growth in the medical device industry. A silhouetted figure points to a glowing dollar sign on a rising graph, symbolizing successful funding strategies. The design is complemented by floating dollar signs and a sleek, modern digital aesthetic.

    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.

  • Filter Integrity Biopharmaceutical Manufacturing

    Filter Integrity Biopharmaceutical Manufacturing explores the relationship between microbial retention tests and integrity tests essential for validating the effectiveness of filters in critical applications.

  • Biocompatibility Evaluation ISO 10993-1 Accessibility Alt description: FDA sign in front of FDA building that says "U.S. Department of. health and Human Services Food and Drug Administration"

    Review of FDA Guidance on Using ISO 10993-1 integrating biocompatibility evaluation within the risk management process, as outlined in the FDA Guidance Document  Use of International Standard ISO 10993-1, Biological Evaluation of Medical Devices Part 1: Evaluation and testing within a risk management process.

  • Service Design Medical Device Development Description: Healthcare worker looking at screen of her equipment

    Integrating service design with user-centered design when developing medical devices can enhance device usability, efficiency, and outcomes.

  • Voice of the Customer Medical Device Research

    7 Tips for conducting Voice of Customer medical device research in Low- and Middle- Income Countries (LMICs) is an integral component in user-centric design and development. It is increasingly an expectation of regulatory bodies.