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EVENT DATE
Oct 2016
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Validation of GC/ GC-MS methodologies - By Compliance Global Inc.

Online Event
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Overview

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

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.

For more detail please click on this below link:

http://bit.ly/2ckJNlW

Email: referrals@complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515

Fax: +1-516-900-5510

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