HPLC Analytical Method Development and Validation

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Dr. John C. Fetzer

Speaker: Dr. John C. Fetzer

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FDA Compliance Webinar Image
Date
09 July, 2026 (Thursday)
Time
10:00 AM PDT | 01:00 PM EDT
Duration
60 Minutes

Overview

Instrumental liquid chromatography is an analysis widely used to determine purity, impurities, and the degradation products of pharmaceuticals.

The focus of most validation work is on the methodology, the standard operating procedure (SOP). But validation of the instrumentation and other associated items of column, solvents, and other reagents and chemicals is also an area of focus in an audit.

Why Should You Attend


In order to meet US EPA or FDA requirements, a method must meet many stringent requirements. The more important of these specific analytical methods are method validation and instrument validation. To not do so is a non-compliance in which any data is not usable or reportable.

Who Will Benefit?

Chemists and Laboratory Assistants who Perform HPLC or UPLC Analyses Under GLP or ISO 17025

Speaker

Dr. John C. Fetzer has been doing liquid chromatographic method development for over 35 years. His PhD was in studies of various types of chromatography. He has authored or co-authored over 50 papers on LC separations, has served on the advisory boards of the Journal of Chromatography, Analytical Chemistry, and Analytical and Bioanalytical Chemistry. He supervised the Good Laboratory Practices accreditation of a large research chromatography laboratory and has taught numerous short courses on GLP and ISO 17025 compliance. 
 

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