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Articles by Suzanne Kuiper
11.25.25 -- Considerations In Sterility Testing And Assurance
Webinar: When a Logbook Project Becomes a Digital Movement Discover how Jazz Pharmaceuticals modernized GMP operations with Tulip's composable platform. Starting with digital logbooks and rapidly expanding into scheduling, calibration, and cleaning validation, Jazz boosted execution speed and compliance without MES complexity.
Global Industry Solutions for a Global Plastics Treaty
Get the latest KPMG thought leadership directly to your individual personalized dashboard Home › Insights › Global Industry Solutions for a Global Plastics Treaty The significant increase in plastic pollution is an environmental crisis of our time. In March 2022, 175 member states adopted a historic resolution at the fifth session of the United Nations Environment Assembly (UNEA-5.2), to develop an international, legally binding agreement on plastic pollution, including in the marine environment.
Preparing the road to circular economy reporting
In a circular economy, companies are incentivized to reuse products and components, minimize use of scarce resources, reduce greenhouse gas emissions (GHG), waste and pollution, and treat the environment with respect, to regenerate nature. The WBCSD Circular Transition Indicators (CTI) provide companies with a framework for measuring circularity, to support decision making and transparency in the transition towards a more circular business.
Comparing Methods For Residual Moisture Analysis Of Lyophilized Products
By Suzanne Kuiper, PhD, Lighthouse Instruments Many biopharmaceuticals rely on freeze drying to extend the shelf-life of these valuable materials. The residual moisture content after freeze drying is a critical product parameter since it can impact the reconstitution time, cake appearance and physical stability of the final product.
Test Method Development For A Container Closure Integrity Test Using Headspace Gas Ingress
By Suzanne Kuiper, Ph.D., Lighthouse Instruments To ensure patient safety, good container closure integrity (CCI) is of great importance for all sterile injectable products. Good CCI prevents ingress of contaminants, such as microorganisms and gases, that can negatively affect product sterility and/or efficacy. Not all defects that can cause a loss in CCI can be detected using visual inspection processes.
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