Quality Control

1. Nitrosamine Impurities Deadline: Are Your Products Compliant? 12/5/2023

   Learn how to select an experienced nitrosamine mitigation provider and how a tailored, quantified strategy can help you bring your product into compliance while maintaining control of the process.

2. Test Method Migration Considerations For CCIT 4/14/2020

   In this webinar you'll learn how to assess test method accuracy, information, and data analysis, how to carefully define method transfer objectives for each application, and more. 

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. 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. 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.

6. Rapid Microbial Detection System For Earlier Results 4/7/2022

   Learn about the Milliflex® Quantum system, a fluorescence-based microbial detection system that enables you to read results days earlier than traditional methods.

7. 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.

8. 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.

9. 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.

10. 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.