When: |
23 Jan through 23 Jan 2019 | |
Where: |
Online Event | United States | |
Website URL: |
https://bit.ly/2Rdk9WS | |
Sponsoring organization: |
Training Doyens | |
Categories: |
Life Sciences - Biotechnology/ Bioinformatics |
Keywords:
Event description:
OVERVIEW
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 ...
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Posting date:
14 January 2019 | 138 views
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