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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  • Detailed 3D rendering of human facial muscles. A visual guide to the complex anatomy of the face and neck.

    Tissue Simulation: Advances for Next-Gen Medical Devices

    Today, 85% of the top 50 healthcare companies use Computational Modeling and Simulation (CM&S) to develop their products and processes. Whether it’s refining overall device parameters or optimizing critical requirements, engineering simulations help reduce development timelines and enhance design exploration.

  • A man in a checkered shirt stands and points to a 3D CAD model displayed on a large monitor. The model shows the internal layout of a device with visible components and structural details in purple and white. To the left of the man, bold black text reads “Why Front-End Research matters,” with a large red arrow curving up toward the screen. The background is a clean white, emphasizing the visual focus on the monitor and text.

    Contextual Inquiry in MedTech: Observe Before You Build

    Paul Charlebois and Eric Olson explore how contextual inquiry in MedTech drives smarter product design. By observing how users interact with devices in real settings, product teams can gather early insights that shape usability, adoption, and safety—long before development begins.

  • FDA use of AI in medical device review - A computer chip labeled "AI" on the left side is connected by a black arrow pointing to the right, where wooden blocks stacked vertically spell out "FDA." Above the image is a bold caption that says "They're doing it!" in white text on a black background. The image suggests the FDA is adopting AI technology.

    How the FDA Is Using AI in Regulatory Review

    Ariana Wilson and Mark Drlik dive into how the FDA is adopting artificial intelligence to modernize its regulatory processes. With a new chief AI officer in place and rumors of collaboration with OpenAI, the agency is taking major steps to automate review workflows and improve efficiency.

  • A laboratory or engineering workstation featuring a high-precision stereo microscope mounted on an articulated arm, positioned beside two computer monitors displaying 3D CAD models or imaging of a complex mechanical or biomedical device. The workspace also includes a keyboard, mouse, and a metallic container, all situated on a clean white desk in a dimly lit, modern lab environment.

    Computational Modelling and Simulation in Medical Device Development

    In a sophisticated world of ever increasing complexity, we need our tools to evolve alongside us and assist in complex decision making, allowing us to understand the consequences of choices ahead. Computational Modelling and Simulation (CM&S) is emerging as an essential tool in building evidence for medical device development.

  • A row of metallic hex nuts anodized in vibrant colors including blue, pink, purple, and gold are arranged on a white surface. To the left, bold purple text reads "Illusion of Color," suggesting a theme about visual perception or surface treatment.

    How Anodized Titanium Enhances Medical Devices with Structural Color

    We explore the fascinating intersection of materials science and usability in medical device development. Mark Drlik and Ariana Wilson discuss how anodized titanium produces vibrant color without dyes, and how this visual property supports surgical safety, device differentiation, and biocompatibility.

  • A laptop on a wooden desk displays a digital document icon on its screen. Beside it, bold text reads "Design History Files Explained," highlighting the topic of regulatory documentation in medical device development.

    Bio Break: Why the Design History File (DHF) Matters in MedTech

    Nick and Joris break down what a DHF is, why it's required, and how it plays a vital role throughout the development lifecycle.

  • A visual project roadmap titled "Finding the Path to MedTech Innovation" shows five development phases: Phase Zero (Pathfinder Product Definition), Phase One (Engineering Detailed Design), Phase Two (Transfer), and Phase Three (Manufacturing). Each phase includes activities such as contextual research, usability engineering, IP generation, design input development, regulatory strategy, prototyping, verification, manufacturing process development, and volume manufacturing. Arrows represent workflows across multiple functions like product development, quality, and regulatory support, with milestone gates marked by stars.

    Bio Break: Finding the Path to MedTech Innovation with the Pathfinder Program

    Nick and Joris explore one of the most dynamic early-phase services at StarFish Medical: the Pathfinder Program. If you're a medtech innovator with a promising concept or prototype, Pathfinder helps you identify the right path forward—before you invest millions in development.

  • A stylized dart hits the center of a yellow target next to bold text reading "Future of Ablation Technology" on a white background.

    Bio Break: Types of Ablation

    Nick and Joris explore the wide world of ablation technologies—unpacking how each approach works and what it’s best suited for.

  • Close-up of gloved hands holding a medical catheter with the text "Minimally Invasive Maximum Impact" on the right side, representing advanced medical device technology.

    Bio Break: How Ablation Technology Is Transforming Surgery

    Nick Allan and Joris van der Heijden dive into one of the most impactful trends in modern medtech: minimally invasive surgery. Ablation technology plays a crucial role as hospitals and healthcare providers aim to reduce patient recovery times and overall system strain.