BEGIN:VCALENDAR X-WR-TIMEZONE:US/Eastern DTSTART:20190123T130000 DTEND:20190123T140000 VERSION:2.0 LOCATION:OnlinePRODID:-//Training Doyens //EN METHOD:REQUEST BEGIN:VEVENT UID:20190123T000000-1062985284-example.com DTSTAMP:20190123T000000 DTSTART;TZID="US/Eastern":20190123T130000 DTEND;TZID="US/Eastern":20190123T140000 SUMMARY:Instrumental Issues in the Validation of HPLC/UPLC Methodologies DESCRIPTION: 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. PRIORITY:3END:VEVENT END:VCALENDAR