Despite the benefits of container closure integrity testing methods, there is no one-size -fits-all solution to evaluate all the types of primary packaging. Additionally, the pharmaceutical and ...

Dublin, Sept. 23, 2025 (GLOBE NEWSWIRE) -- The "Container Closure Integrity Testing Market Industry Trends and Global Forecasts to 2035: Distribution by Type of Container Tested (Vials, Syringes, and ...

All sterile drug manufacturer is required to check and demonstrate their manufacturing systems capable of maintaining container and closure barrier integrity throughout the product life cycle. As such ...

This webinar will cover how headspace testing methods are developed and validated for a variety of product-container configurations, including assembled autoinjectors. It has become generally accepted ...

The revised USP Chapter Sterile Product Packaging-Integrity Evaluation gives best practices for obtaining reliable data in container closure integrity testing and recommends quantitative deterministic ...

At different stages of the drug lifecycle, the minimum provision for parenteral products is a safety barrier against potential contaminants. This protection is guaranteed by selected container closure ...

The pharmaceutical and biotech industries face many challenges when selecting the appropriate stopper, seal, and vial combination for a drug product. Further compounding these challenges is the ...

The Indian pharmaceutical industry is of the view that the recent US FDA norms on container closure system will enhance quality and reliability of drug’s shelf-life. The manufacturers emphasize that ...

Pfeiffer Vacuum introduces an innovative addition to both new and existing leak detection systems: the Dry Chiller Module. Serving as an extended cooling component for ASM 2000 and AMI 1000 leak ...