Quality Control

  1. 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.

  2. Using Positive Controls In Container Closure Integrity Studies 1/2/2019

    This webinar describes the use of positive controls as an important element of CCI studies designed to validate packaging components for CCI or to qualify processes for producing good CCI.

  3. Data Integrity In The Quality Control Lab: No Pen, No Pain 12/10/2024

    Data integrity in pharmaceutical QC labs is critical for product safety. This webinar explores digital solutions to improve traceability, reduce paperwork, and enhance workflows.

  4. 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.

  5. An Efficient And Reliable Way To Digitalize Your Sterility And QC Testing Data 5/2/2023

    Watch to learn about the M-Trace™ Electronic Test Record Software, your digital QC companion for trusted and efficient data recording that automizes and digitalizes your sterility and QC testing data.

  6. The Route To Faster Microbial Quality Control 6/7/2023

    Join product and application experts Anne-Grit Klees, Carine Krebs, and Esther Welterlin to discover the benefits of using a new rapid microbial detection platform.

  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. 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.

  9. 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.

  10. 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.