Introduction
Quality assurance and quality control are key components of every pharmaceutical manufacturing. To meet the standards set by U.S. Pharmacopeia (USP) <232> and the International Council for Harmonization (ICH) Q3D, QA/QC labs performing routine trace-elemental analyses must rely on precise and reliable data while also adhering to the stringent U.S. FDA 21 CFR Part 11 data security requirements. Additionally, utilizing dependable and user-friendly testing solutions enables labs to efficiently meet their throughput demands.
This webinar explores the latest innovations in ICP-MS technology, designed to meet or exceed the requirements of pharma QA/QC labs performing routine trace-elemental analyses. It also covers available qualification protocols and services for laboratory instrumentation, ensuring complete, consistent, and accurate data.
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