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HPLC Method Transfers by Applying USP 621

RECORD | Already taken place Th, 1.5.2025
In this webinar, we will give an overview of Chromatography General Chapter <621> and allowed adjustments to specific chromatographic systems in the USP monographs based on the revised General Chapter <621>.
Go to the webinar
Agilent Technologies: Navigation Pharma Regulations: Insight and Innovations
Agilent Technologies: Navigation Pharma Regulations: Insight and Innovations

General Chapter <621> is one of the most important USP general chapters, impacting most of the USP monographs related to chromatography.

Establishing meaningful system suitability criteria for chromatography procedures is a key requirement of compendial and regulatory compliance. This general chapter describes CQAs and the extent of modifications that can be done to the compendial methods if the system suitability criteria are met or exceeded.

In this webinar, we will give an overview of Chromatography General Chapter <621> and allowed adjustments to specific chromatographic systems in the USP monographs based on the revised General Chapter <621>.

By attending this webinar session, you will understand, what these changes are & how these changes will impact chromatography. We will also discuss expertise and solutions Agilent can offer to profit from these changes by modernizing the analytical methods, improving productivity, reducing cost of analysis.

Presenter: Carl Griffin (LC Columns Applications Scientist, Agilent Technologies, Inc.)

Carl Griffin is an Application Engineer for HPLC column chemistry at Agilent. He started his career as an organic chemist in the pharmaceutical industry but left it several decades ago to be involved in analytical and preparative chromatography. As he says, I’ve worked on small and large molecules at both analytical and preparative scales. Currently Carl is involved with method development, product support, troubleshooting, and educating in HPLC for eastern North America.

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