Quality White Papers & Case Studies

  1. What Pharmacies Often Miss In USP <800> Compliance 5/27/2026

    Master USP <800> compliance by transitioning from standalone equipment to an integrated system design. Review key protocols for a multi-layered strategy to mitigate cumulative drug risks.

  2. Isolator Integration In Cell And Gene Therapy Manufacturing 5/27/2026

    Safeguard living medicines with a tailored facility design strategy. Evaluate workflows with this six-dimensional model against your CCS for a holistic look to inform your decisions.

  3. Pouching Solutions For Sterile And Moisture-Sensitive Devices 5/20/2026

    Aseptic pouching requires specialized mechanical segregation and sterile vacuum handling. Discover how targeted engineering maintains Grade A compliance.

  4. Effective Strategies To Minimize Product Loss During Fill Finish 5/11/2026

    Every drop of high-value biologic lost in fill finish is money left on the table. Learn practical strategies to protect your yield.

  5. How A Global Biosimilars Company Cut Manual Data Errors By 50% 5/8/2026

    Learn how a global biopharmaceutical leader halved transcription errors and integrated over 350 instruments to accelerate the development of high-quality, clinically proven biosimilars.

  6. Predicting Performance Of Lotions Through Rheological Characterization 5/6/2026

    Rheological testing shows how small formulation differences influence spreading, flow, and feel during use. With minimal sample volumes, these methods connect lab measurements to real‑world performance.

  7. Rheology Is An Accurate Predictor Of Pharmaceutical Lotion Stability 5/6/2026

    Rheological creep testing provides a rapid way to predict pharmaceutical lotion stability by linking steady-state viscosity to particle settling behavior, enabling reliable shelf-life estimates.

  8. Precision Polymorph Screening With Electron Diffraction 5/6/2026

    See how polymorph screening with electron diffraction uncovers hidden forms, enabling precise identification and reliable quantification of minor phases affecting performance and manufacturability.

  9. Mechanochemistry- Enabled Solid-State Stress Testing 5/6/2026

    Discover how solvent‑free, solid‑state stress testing speeds degradation studies, yields realistic impurity profiles, and provides earlier, material‑efficient insight into drug stability and risk.

  10. (Cross-) Contamination Control Through Effective Equipment Cleaning 5/6/2026

    Discover science-driven cleaning strategies that reduce cross-contamination, enable safe multiproduct manufacturing, and support faster, flexible GMP changeovers.