Articles By Eric Larson

  1. West Vantage™ Goes Beyond Contract Manufacturing 4/23/2026

    Successfully advancing a drug-delivery device to market demands more than technical expertise; it requires coordinated execution, regulatory insight, and the ability to scale without disruption.

  2. Selecting The Right eQMS To Maximize Quality Maturity 4/23/2026

    Let's take a closer look at the current electronic quality management system (eQMS) landscape in pharma/biotech and what a future-ready eQMS must enable to support continuous improvement.

  3. Own Your Digital Sovereignty: A Diagnostic Guide For Manufacturers 4/22/2026

    Stable systems can still resist change. Learn how to assess whether your manufacturing architecture can evolve safely, scale new capabilities, and keep validation from quietly slowing progress.

  4. Package With A Purpose 4/21/2026

    Packaging shapes how devices are understood, handled, and used. A human-centered approach surfaces critical info sooner, reduces errors, and strengthens safety and usability.

  5. Safeguarding Biologic Integrity Through Enhanced Component Compatibility 4/21/2026

    For sensitive biologics and viral vectors, risk extends beyond simple contamination. Utilizing inert barrier films on contact surfaces reduces compound migration and adsorption, maintaining dosage accuracy.

  6. Optimizing Syringe Performance For Reliable Drug Delivery 4/21/2026

    Reliable drug delivery requires precision. Maintaining a robust seal throughout a product’s shelf life is essential to preserve sterility and ensure patient safety during self-administration.

  7. Maintaining Sterility Through Precise Component Design And Manufacture 4/21/2026

    Prioritizing high-quality component design and manufacturing excellence can mitigate risks, ensure long-term container closure integrity, and avoid the costly delays associated with non-compliance.

  8. 04.21.26 -- Preventing Medical Device Recalls Starts With Supplier Quality 4/21/2026
    04/21/26 Med Device Online Newsletter
  9. How Regulatory Is Becoming An Increasingly Valuable Asset 4/20/2026

    Build regulatory strategy into your company from day one — not as support, but as a core driver of value, risk management, and successful commercialization.

  10. A New Standard For Production Efficiency And GxP Compliance 4/20/2026

    Traditional MES platforms were built for stable environments that no longer exist. Manufacturers are now adopting composable execution architectures to reduce friction and adapt faster.