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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  • Minimum Viable Product Medical Device
  • 12 Steps to Set up a Biomed Lab

    Opening a biomed lab includes managing multi-layer organizational involvement all the way from facilities to the head of operations. When starting a new lab from scratch, the first step is to fully understand the organization’s mission and business goals. This will impact how you approach setup and any purchasing decisions you make. This article describes 12 essential steps to set up a biomed lab.

  • Medical Device Speed to Market

    Speed to market is a crucial part of medical device success. Experts draw upon their experience with hundreds of medical device products for proven tips and recommendations that increase medical device speed to market without sacrificing safety or quality.

  • QNX Medical Device Bootscreen

    QNX Medical Device Bootscreen tips for the popular micro-kernel OS designed for embedded systems and safety critical hardware.

  • Using AI In Medical Devices

    Risks, potential roles, and tips for using Large Language Models (LLM) or (AI) in medical devices effectively and responsibly. Role of AI in medical devices: In the medical field, generative language models, colloquially known as “AI” or “LLM” must be used responsibly to enhance the skills of clinicians or improve patient experience without exposing either to increased risk.

  • Medical Device Design for Testability

    Medical Device Design for Testability during development explores the pros and cons of its application throughout the entire design process design concern throughout the whole design process, ensuring that all parts of the product can be both manipulated and monitored allowing for thorough testing.

  • biomedical product development

    Three common elements can be observed in biomedical product development projects that are doomed to failure. They are the Three “P’s” – Platform, Point of Care, and Program Manager.

  • ESG Medical Device Impact

    Environmental, Social and Governance (ESG) Medical Device Impact tips to ensure that your products fulfill compliance obligations. Major buyers request ESG reporting from suppliers as new and revised regulations require supply chain attention.

  • Gender Equity Medical Device

    Gender data gap’s implications on women’s health and strategic measures for its integration into gender gap medical devices, regulatory frameworks and design processes.