Agilent Life Sciences USP 232 Class1 and 2 Parenteral Elements
The Agilent 5191-4533 USP 232 Class 1 and 2 Parenteral Elements Standard is designed for use in elemental impurity analysis in accordance with United States Pharmacopeia (USP) <232> guidelines. This certified reference material contains a mixture of Class 1 and 2 elements commonly monitored in pharmaceutical products, supporting compliance with regulatory requirements for parenteral drug products. The standard is manufactured and quality-assured by Agilent to ensure accuracy and traceability, making it suitable for calibration and validation of analytical methods such as ICP-MS and ICP-OES.
