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Validation of GC/ GC-MS methodologies - By Compliance Global Inc.
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.
• Instrument Validation
o The gas system
o The injector
o The column
o The detection system
o The data system
• Method Validation
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 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
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.
For more detail please click on this below link:
Toll Free: +1-844-746-4244
Contact the event managers listed below for more information about how you can participate at the Validation of GC/ GC-MS methodologies - By Compliance Global Inc..
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
Compliance Global Inc.
Compliance Global Inc. http://www.seatradecruiseglobal.com/sponsorship-opportunities
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