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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  • 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.

    Bio Break: Pros and Cons of Platform Technologies in Medical Device Development

    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?

  • Medical Device Curate Community and Innovation

    Medical Device Innovation Initiatives

    We design medical devices and our medical device innovation initiatives support the energy and shared passion when team members work together in person.

  • Company Culture and Values

    Peer Kudos Reflect Company Culture and Values

    A selection of Peer Kudos from the past year or two that say a lot about our company culture and values.

  • Elearning LMS Medical Device

    How eLearning and LMS Empower Medical Device Employees

    elearning and LMS improve an employee’s ability to learn and adhere to the company QMS for medical device design and development.

  • Sharing Using Superpowers Kryptonite

    Sharing and Using SuperPowers and Kryptonite

    Our SuperPowers and Kryptonite program will continue to develop over time. It fosters a culture where people are inspired and able to do the most fulfilling work of their lives.

  • 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."

    Bio Break: The Van Halen Secret to Medical Device Safety

    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.

    Bio Break: Funding Strategies for Medical Devices

    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

    Validating Filter Integrity for 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"

    FDA Guidance on Biocompatibility Evaluation ISO 10993-1

    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.