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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  • A stethoscope placed on a glowing digital circuit board, symbolizing the intersection of healthcare and technology in medical device innovation.

    In the fast-paced world of medical device development, ensuring a smooth design transfer is critical for product success. However, a common pitfall arises when limits around essential performance are not well defined. In his recent article for Medical Product Outsourcing (MPO), Dana Trousil, StarFish Medical’s Mechanical Engineering Team Manager, dives into the challenges and solutions for addressing these issues.

  • 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.

  • Medical Device Manufacturing Tips

    33 tips and examples from commercialization experts for manufacturing a medical device.

  • UDI Labels Medical Devices

    Considerations for designing UDI labels for medical devices include ANSI/ISO Parameter Values, label verification and durability.

  • Medical Device Blog Articles

    Two new blog join eight from last year’s top 10 on the list of most-read StarFish medical device blogs and articles for 2022.

  • The image shows a person wearing safety goggles and a lab coat working at a desk in a laboratory or engineering workspace. They are seated at a computer station with multiple monitors, typing on a keyboard while focusing on the screen. The desk is equipped with tools, documents, and a red organizer tray. The background features shelves and technical equipment, indicating a controlled, professional environment for research, development, or testing purposes.

    Writing and implementing standard operating procedures (SOPs) for the manufacture of medical devices is required by ISO 13485, FDA, and other regulatory bodies. An SOP is a set of written instructions that documents a routine or repetitive activity that is followed by employees in an organization. The development and use of SOPs are integral parts of a successful quality system. They provide directions to perform a job properly and consistently to achieve predetermined specifications and quality end results. SOPs address all requirements to complete the job or process safely and effectively.

  • Device Design Tolerance Studies

    Examples of how to apply tolerance studies that add value to medical device design and ultimately to biomedical start-ups.

  • What Attracted These Employees to StarFish Medical?

    What Attracts Employees StarFish Medical? Employees share expectations prior to joining with experiences being part of StarFish.

  • Future of BioManufacturing

    Six BioManufacturing Trends to Watch in 2022 and the future of BioManufacturing analyzed by Bioscience and medical device experts.