Validation of GC/ GC-MS methodologies - By Compliance Global Inc
About This Event
Overview :
Instrumental gas chromatography, either as GC or GC-MS, are common techniques in laboratories that do regulatory-compliance work.
Why Should You Attend :
In order to meet US EPA or FDA requirements, a method must meet many stringent requirements.
Areas Covered in this Webinar :
The more important of these for specific analytical methods are method validation and instrument validation. To not do so is a non-compliance in which any data is not usable or reportable.
Learning Objectives :
• Instrument Validation
o The gas system
o The injector
o The column
o The detection system
o The data system
• Method Validation
o Accuracy
o Precision and the various measures of precision (repeatability, reproducibility, ruggedness, robustness)
o Limits of detection and quantitation, linearity
o Selectivity, interferences, and specificity
o Sensitivity
o Solution stability
Who Will Benefit :
• Lab Chemists
• Lab Managers
• Lab Technicians
• Lab Analysts
• Industries into Compliance Methodology (Biotech, Pharma) Companies into Environmental Compliance or EPA
• Chemists and Laboratory Assistants who perform HPLC or UPLC analyses under GLP or ISO 17025
For more information, please visit : https://www.complianceglobal.us/product/700570/JohnCFetzer/validation-of-gc-gc-ms-methodologies%20/1
Email: [email protected]
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
Level:
Intermediate
Speaker Profile :
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.