Articles By Eric Larson

  1. 06.02.26 -- Will FDA's One-Day Inspection Pilot Ease The Backlog? 6/2/2026
    06/02/26 Med Device Online Newsletter
  2. What Is Computer Software Assurance, And What Are Its Benefits? 6/2/2026

    Kamila Novak reviews final computer software assurance (CSA) guidance and what it means for those working on medical device clinical trials.

  3. 05.31.26 -- Why Are Life Science Companies So Poorly Prepared For RIM's Future? 5/31/2026

    05/31/26 Med Device Online Newsletter

  4. Risk Is the Spine: What The First 100 QMSR Inspections Reveal 5/29/2026

    The FDA has now completed just over 100 inspections under its new Quality Management System Regulation, and the agency has begun sharing preliminary observations from those inspections.

  5. Small Joint Implants: A New Era With Medureon™ Bionate 5/27/2026

    Advances in biomaterials address challenges of small joint implants, improving durability, flexibility, and biocompatibility to reduce wear, enhance motion, and support long‑term patient outcomes.

  6. The Role Of Processing And Supplier Diversification 5/26/2026

    Optimizing UHMWPE implants requires balancing materials, processing, and sourcing to improve performance, reduce risk, and lower costs in medical device manufacturing.

  7. 05.26.26 -- Extending Care When Minutes Matter 5/26/2026

    05/26/26 Med Device Online Newsletter

  8. 05.26.26 -- Preparing RIM Strategies For What's Next 5/26/2026

    05/26/26 Med Device Online Newsletter

  9. 05.24.26 -- Complaints Into Practical Action: Human Factors Drug Delivery 5/24/2026

    05/24/26 Med Device Online Newsletter

  10. Turn Regulatory Readiness Into An Operational Advantage 5/22/2026

    Paper-based GxP workflows hide risk and stall progress. Learn how embedding compliance into digital execution creates real-time traceability and turns regulatory readiness into an advantage.