Quality White Papers & Case Studies

  1. (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.

  2. Why Pharmaceutical Scientists Trust The Discovery Core Rheometer 5/1/2026

    Drug formulations demand more than single‑point viscosity data. Explore how rheology reveals stability, flow, and structural behavior across suspensions, topicals, and injectables.

  3. Standardized Extraction Protocol Per USP <665>: Bridging Regulatory Expectations And Industry Best Practices 4/29/2026

    View how to implement USP <665> extractables testing, align with global E&L standards, and apply risk-based strategies to ensure regulatory compliance and patient safety.

  4. Stability With IDBS Polar 4/24/2026

    Manual tracking often leads to missed pulls and data gaps. Discover how a connected digital workflow governs stability execution, ensuring consistency and regulatory confidence at every timepoint.

  5. Robust, High-Throughput Automated Solution For Water Endotoxin Testing 4/21/2026

    High-throughput water endotoxin testing doesn’t have to sacrifice consistency. Gain insight into how an automated workflow delivers reliable results, low variability, and strong control recovery.

  6. Global Regulatory Harmonization: Comparisons In Aseptic Barrier Systems 4/20/2026

    Compare global aseptic standards from the FDA, EMA, PIC/S, and WHO. Gain insights into how advanced barrier systems harmonize international requirements to ensure sterile product integrity and safety.

  7. Shielded BSCs: Regulatory Requirement Or Risk-Based Engineering Solution? 4/20/2026

    Master the balance between USP <825> aseptic standards and radiation safety. Learn how integrated engineering solutions ensure regulatory compliance while protecting both patients and personnel.

  8. ADC Development Grows More Complex — SPR Insights Bring Clarity 4/14/2026

    Explore how real-time kinetic analysis reveals how conjugation, linker chemistry, and drug loading influence antibody–antigen interactions, while enabling sensitive detection of anti-drug antibodies.

  9. The Open Standard For Plug-And-Produce 4/14/2026

    Take a look at how standardized, modular production simplifies line integration, reduces engineering effort, and enables faster changeovers. Ideal for teams seeking flexible manufacturing models.

  10. Safely Scaling High Potency API Manufacturing 4/13/2026

    Scaling HPAPI production demands disciplined containment and exposure control. Integrated operating models help manage risk while enabling compliant, reliable scale‑up.