USP <1031>: The Decision Framework Pharmaceutical Packaging Teams Have Been Missing For many years, pharmaceutical packaging teams faced a familiar Read More
USP <87> Is Changing — What the Expanded In Vitro Framework Means for Pharmaceutical Packaging USP <87> has long been associated with cytotoxicity testing, Read More
Why Pharmaceutical Packaging Biocompatibility Is Moving Beyond Checklists For decades, biocompatibility testing for pharmaceutical packaging followed a Read More
USP <87> Biological Reactivity (In Vitro): A Smart Cytotoxicity Screen for Plastics & Elastomers; From Early Characterization to Release Biocompatibility isn’t a box to check; it’s a continuous Read More
Food and Drug Administration Testing Requirements for Pre-filled Syringes The Food and Drug Administration (FDA) plays a crucial Read More
The Use of Pre-filled Syringes for Drug Products: Enhancing Patient Safety and Convenience The pharmaceutical industry continues to evolve, introducing innovations aimed Read More
Understanding the New European Pharmacopoeia 2.4.35 Chapter for Elemental Impurities in Plastic Materials Author: Ronak Patel, Analytical Chemistry Manager Elemental impurities in Read More
The Sample Intake Process: Ensuring Accuracy and Efficiency Written By Jacqueline Zsoldos / Quality Administrator When samples Read More
Understanding Cleaning Validation in Pharmaceutical Manufacturing Written By Ronak Patel / Manager, Analytical Chemistry Cleaning Read More
