
Application Note
Perform Compliant USP 232 and ICH Q3D Elemental Analysis

Application Note
Perform Compliant USP 232 and ICH Q3D Elemental Analysis
Elemental impurities in pharmaceutical formulations can interfere with drug efficacy or have a toxic effect on the patient. Regulators have issued guidelines—such as ICH Q3D, USP 232 and USP 233 Elemental Impurities.
Download this application compendium to learn how to monitor a range of metal elemental impurities in pharmaceutical materials using elemental analysis techniques such as:
- ICP-OES
- ICP-MS or,
- AAS
As well as tips to ensure specific validation requirements described in the guidelines are met.
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