Quality Control

  1. 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.

  2. Minimizing Particulate Risk 5/13/2026

    While visible particles often draw immediate attention, visual inspection alone is insufficient, as subvisible particulate matter can pose equally significant risks to patient safety.

  3. 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.

  4. Container Closure Integrity Testing Technologies - PTI Packaging Technologies & Inspection 9/2/2020

    PTI-Packaging Technologies & Inspection is headquartered in Hawthorne, New York, a Westchester county community close to New York City. We are a team of engineers, scientists and professionals serving the packaging industry as a leading equipment manufacturer of package inspection equipment. PTI’s inspection technologies are deterministic test methods that produce quantitative test result data. Our technologies conform to ASTM and other regulatory standards. We specialize in offering our customers the entire solution including test method development and packaging inspection equipment validation. PTI installations have been successful in globally transferable and validated test methods.

  5. 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.

  6. Quality Time With Oliver: Guest - Dave Exline 10/5/2026

    Particulate analysis and Container Closure Integrity Testing determine whether a pharmaceutical batch holds up under regulatory scrutiny, and why a single flawed reading can carry real consequences.

  7. 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.

  8. Mitigating Ultracold Storage And Transport Risk With CCIT

    Dr. Derek Duncan, Director of Product Lines, Lighthouse Instruments, and Brandon Zurawlow, Chief Scientific Officer, CS Analytical, discuss a program for generating packaging data for deep cold storage products.

  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. 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.