Quality Control

  1. The Future Of Robotics And Automation In QC In Microbial Testing Labs 4/7/2022

    Automation based on the use of robotics and digital tools will transform the QC process in microbial testing labs to meet the productivity, data integrity, and reliability requirements of Pharma 4.0.

  2. Bioburden And EU GMP Annex 1: Risk Assessment, Reduction, And Testing

    Experts on regulation, filtration, sampling, and quality control discuss risk assessment and filtration-based strategies to reduce bioburden.

  3. Making Sense Of Analytical Standards In Pharma QC

    Reference materials are a critical component of the analytical testing workflow. Learn about metrological traceability, the hierarchy of reference materials, fit-for-purpose selection considerations, and more.

  4. Workflow For Rapid Sterility Testing 4/14/2023

    Learn about the workflow for an automated solution for the rapid detection, imaging, and quantification of viable microbial contaminants in filterable samples at various stages of the manufacturing process.

  5. Microbial Sampling Of Compressed Gas Has Never Been So Simple And Safe 4/3/2023

    Discover the key features of an innovative microbial compressed gas air sampler, designed for the user's peace of mind, ease of use, maximum safety, and full regulatory compliance.

  6. Selecting Container Closure Components: Extractables And Leachables

    Primary packaging components require a thorough assessment to ensure safety and efficacy. Plan ahead and start your assessment early to mitigate your risks, delays, and out-of-pocket costs.

  7. 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.

  8. Container Closure Integrity Testing Method Development

    Dr. Derek Duncan, Director of Product Lines, Lighthouse Instruments, covers approaches that can be used for method development for CCI testing in all phases of the product life cycle.

  9. Compressed Gas Risk Assessment: A Significant Step In Your CCS 10/10/2024

    Discover the importance of compressed gas monitoring in ensuring product quality and compliance with EU GMP standards.

  10. Determining CCI During Deep Cold Storage 7/23/2020

    Deep cold storage, at dry ice (-80°C) or even cryogenic (-196 °C) temperatures, poses a significant challenge to packaging components and can result in CCI failures.