Quality Assurance

  1. Airflow Visualization Studies: The Impact Of Annex 1 On Sterility Assurance 12/18/2024

    Airflow visualization techniques like Smoke Studies and CFD analyses are crucial for contamination control, aiding cleanroom qualification, environmental monitoring, and optimizing contamination control strategies under Annex 1.

  2. Meet The Experts: PAT, Raman Spectroscopy, And Chemometrics 4/14/2023

    Gain a better understanding of process analytical technology (PAT), Raman spectroscopy, chemometrics, and Raman applications in bioprocessing.

  3. A Rapid Approach For Moisture Determination Of Lyophilized Product 11/13/2024

    Explore the limitations of traditional moisture determination techniques, an innovative approach using laser-based headspace analysis, and real-world case studies using this non-destructive method.

  4. Determining And Controlling Oxygen Levels In Sensitive Formulations 1/2/2019

    This webinar will review how oxygen levels in finished parenteral drug containers can be determined and controlled throughout the product life cycle by using laser-based headspace analysis.

  5. Navigating GxP Compliance Challenges 10/30/2024

    Learn how to select and manage trusted software suppliers to streamline your digital transformation, mitigate risks, and ensure regulatory adherence. Watch to discover best practices and real-world examples.

  6. Solutions In Pre-Filled Syringes For Biologics And Ophthalmic Applications 6/19/2025

    Discover how pharma companies can select tailored pre-filled syringes for biologics and biosimilars by aligning drug delivery needs with specialized containers and analytical services.

  7. CCI Testing And Revisions To EU Annex 1 1/2/2019

    The new language in EU Annex 1 will likely have a significant impact on your CCI testing practices. In this webinar CCI testing strategies and the proposed revisions to EU Annex 1 are discussed.

  8. Multi‑Sample Testing With Precise Failure Detection For Throughput 12/29/2025

    Test multiple samples at once with a multi‑sample testing platform that ensures accurate detection for low headspace formats and integrates into automated lines for high-volume efficiency.

  9. The Sensitivity Trap: Building Confidence In CCIT Performance 3/2/2026

    Effective CCIT goes beyond micron claims, focusing instead on repeatability, confidence, and real‑world relevance. Learn how to define a defensible LOD and understand what auditors truly prioritize.

  10. Autoinjector Testing: Addressing Sensitivity And Headspace Challenges 1/30/2026

    Micron‑level defects can jeopardize autoinjector sterility. Learn how vacuum decay offers a deterministic, repeatable way to verify container integrity and strengthen quality assurance.