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Validation of GC / GC-MS Methodologies - Webinar (Recorded)

  • Webinar

  • 60 Minutes
  • April 2020
  • NetZealous LLC
  • ID: 5004552
Overview:
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 you should 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 Session:
  • The Injector
  • The Column
  • The Detection System
  • The Data System
  • Linearity
  • Selectivity, Interferences, and Specificity
  • Solution Stability
  • Monitoring Performance

Who Will Benefit:
  • Chemist
  • Laboratory Assistants
  • QA Managers and Personnel
  • QC Managers and Personnel
  • Validation Specialists
  • Quality System Auditors
  • Regulatory Compliance Associates

Speaker

John C. Fetzer has had over 30 year experience in HPLC methods development. He has authored or co-authored over 50 peer-reviewed papers onl iquid chromatography, has served on the editorial advisory boards of the Journal of Chromatography, Analytical Chemistry, and Analytical and Bioanalytical Chemistry.

Who Should Attend

  • Chemist
  • Laboratory Assistants
  • QA Managers and Personnel
  • QC Managers and Personnel
  • Validation Specialists
  • Quality System Auditors
  • Regulatory Compliance Associates