This training program will cover in detail the method validation of gas chromatography (GC) and gas chromatography mass spectrometry (GC-MS). It will focus on key elements of validation including injector, column, detection system, data system and much more.
Why Should You Attend:
Instrumental gas chromatography is 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.
This presentation will cover the key elements to have a compliant method.
Areas Covered in the Webinar:
- The Injector
- The Column
- The Detection System
- The Data System
- Linearity
- Selectivity, Interferences, and Specificity
- Solution Stability
- Monitoring Performance
Speakers
Dr John C. Fetzer, PhD,,
Consultant ,
Fetzpahs ConsultingDr. John C. Fetzer has been doing liquid chromatographic method development for over 35 years. His PhD was in studies of various types of chromatography.
He has authored or co-authored over 50 papers on LC separations, has served on the advisory boards of the Journal of Chromatography, Analytical Chemistry, and Analytical and Bioanalytical Chemistry.
He supervised the Good Laboratory Practices accreditation of a large research chromatography laboratory and has taught numerous short courses on GLP and ISO 17025 compliance.
Who Should Attend
- Chemist
- Laboratory Assistants
- QA Managers and Personnel
- QC Managers and Personnel
- Validation Specialists
- Quality System Auditors
- Regulatory Compliance Associates
