Insights On Quality Assurance

  1. Stop Managing CQV In Silos: Unify Your Validation Systems 7/23/2025

    Fragmented CQV systems hinder validation efforts, which risks compliance and slows progress. Discover how centralized platforms streamline processes, boost efficiency, and meet evolving regulatory demands.

  2. The Impact Of The FDA's New CSA Draft Guideline 2/24/2025

    Ensure product quality and patient safety by examining the FDA's draft guideline on Computer Software Assurance that emphasizes a risk-based approach to streamline software validation.

  3. Building A Connected Quality And Manufacturing Ecosystem In Life Sciences 12/27/2024

    Discover the transformative power of connected quality and manufacturing systems, offering strategies for digital transformation, enhanced efficiency, compliance, and real-world success in life sciences.

  4. The CHO Toolkit: Flexible Solutions For Complex Molecules 9/11/2025

    A modular cell line development platform helps overcome biologic complexity. Learn how flexibility and expert support drive success from early development through commercial manufacturing.

  5. Collaboration With Clients 1/29/2025

    If you're looking for a dedicated partner who prioritizes trust, transparent communication, and delivering results that exceed expectations, let's work together to drive your project's success and create lasting impact.

  6. Cambrex Scientist Spotlight: Shawn Conway 1/29/2025

    Shawn Conway, Senior Director of Operations in High Point, NC, leads a dynamic team of engineers and chemists at Cambrex, focused on supporting clients throughout the entire product life cycle.

  7. Your Guide To Precise And Robust Separation Methods 11/12/2025

    Discover a detailed guide to characterizing GLP-1 receptor agonists that covers advanced LC-MS and SEC-MALS workflows for impurity profiling, stability testing, and aggregate analysis.

  8. Master The 2-Point Calibration Process To Maintain Data Integrity 5/19/2025

    Ensure accurate sensor readings with an innovative software by mastering the 2-point calibration process. Learn more about how and why regular calibration supports data integrity and compliance.

  9. A Roadmap For PAT Implementation 7/5/2024

    Through its real-time monitoring and control, PAT supports a proactive approach to quality management, reducing variability and improving the robustness of pharmaceutical production processes.

  10. Handling Protocols: Key Considerations In The Highly Potent API Market 5/12/2025

    Explore the growing role of highly potent active pharmaceutical ingredients in oncology and Antibody-Drug Conjugates to highlight manufacturing challenges, safety protocols, and opportunities for CDMOs.