Time: January 23, 2019 from 1pm to 2pm
Location: Training Doyens 26468 E Walker Dr,Aurora, Colorado
Website or Map: https://bit.ly/2CjEwZr
Event Type: online
Organized By: Training Doyens
Latest Activity: Dec 18, 2018
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.
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.
For more detail please click on this below link:
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