Instrumental Issues in the Validation of HPLC/UPLC methodologies
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Category glp guidelines, glp online training
Deadline: October 18, 2017 | Date: October 18, 2017
Venue/Country: Colorado, U.S.A
Updated: 2017-09-20 13:25:50 (GMT+9)
Call For Papers - CFP
OVERVIEWInstrumental liquid chromatography is an analysis widely used to determine purity, the 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 ATTENDIn order to meet US EPA or FDA requirements, a method must meet many stringent requirements. The more important of these for specific analytical methods are method validation and instrument validation. Not do so, is a non-compliance in which any data is not usable or reportable.AREAS COVERED• Instrument validationo The pumping systemo The columno The detection systemo The Data System• Monitoring for QualityWHO WILL BENEFITChemists and laboratory assistants who perform HPLC or UPLC analyses under GLP or ISO 17025.LEARNING OBJECTIVESInstrumental liquid chromatography, either as HPLC or UPLC, is common techniques 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.For more detail please click on this below link:http://bit.ly/2f5mWMsEmail: supporttrainingdoyens.comToll Free: +1-888-300-8494Tel: +1-720-996-1616Fax: +1-888-909-1882
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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