Insights On Quality Control

  1. From Day One Success To Everyday Improvement: The OR → OE Continuum 11/24/2025

    Bridging the gap between initial startup and long-term sustainability requires a unified strategy. Learn to transform early readiness metrics into a durable operating system that drives continuous performance improvements.

  2. Expanding Capabilities In QC Analyses With Advanced LC Detection 11/26/2024

    Today's quality control (QC) labs need instruments that can accurately take on a wide range of tasks. Discover a system that allows QC labs to enhance their capabilities and achieve various goals.

  3. Accelerate Biologics Product Release With Seamless Viral Testing 6/23/2025

    Explore viral safety testing for biologics, focusing on prevention, detection, and removal strategies, updated regulatory guidance, and common challenges in unprocessed bulk testing.

  4. Leveraging A Modern HPLC System For Peptide Drug Substances Analysis 8/22/2024

    This study assesses a modern HPLC system within a routine QC testing environment focused on peptide-size biopharmaceuticals.

  5. 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.

  6. Digitizing Quality Management: The Key To Avoiding FDA Recalls In Life Sciences 1/13/2025

    Explore the need for digital quality management systems to ensure compliance as life science companies face rising FDA recalls.

  7. Characterizing The Physical Properties Of Spray Dried Powders 10/21/2024

    Ensure the success of your spray-dried powder formulations by thoroughly assessing their physical properties early in the development process to optimize handling, stability, and performance in final dosage forms.

  8. Aggregate Analysis Of Tirzepatide 12/11/2025

    A new size exclusion method effectively analyzes Tirzepatide aggregates, demonstrating robust separation and reproducibility with minimal need for organic solvents or acidic modifiers.

  9. Practical Considerations For Aseptic Gowning In Contamination Control Strategies (CCS) 2/13/2026
  10. Leachables Method Development, Validation And Relevant ICH References 5/16/2025

    It is crucial to develop and validate analytical methods capable of detecting a wide range of potential organic and inorganic leachables specific to the drug and its packaging.