Date(s) - 01/23/2019
Instrumental liquid chromatography, either as HPLC or UPLC, is a common technique in laboratories that do regulatory-compliance work.
For Good Laboratory Practice (GLP) or for ISO 17025 compliance, such methods must meet certain requirements. This presentation will cover the key elements to have a compliant method.
Instrumental liquid chromatography is an analysis widely used to determine purity, the impurities, and the degradation products of pharmaceuticals. The focus of most UPLC and HPLC 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 GLP guidelines or FDA requirements, a method must meet many stringent requirements. The more important of these for specific analytical methods are HPLC and UPLC method validation and instrument validation. To not do so is a non-compliance in which any data is not usable or reportable.
- Instrument validation
- The pumping system
- The column
- The detection system
- The Data System
- Monitoring for Quality
Learn about the specific instrumental issues in UPLC and HPLC method validation.
WHO WILL BENEFIT
Chemists and laboratory assistants who perform HPLC or UPLC analyses under GLP or ISO 17025.
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