WHY SHOULD YOU ATTEND?
Many methodologies are used in more than 1 facility. A common practice is that a method is developed at a R&D laboratory and then transferred to operating facilities to use. It is well known that there can often be no relationships between neither accuracy nor precision values running the same method in different laboratories. The use of universal standards, making operations as identical as possible, round-robin testing, and rigorously uniform training and methods are necessary.AREA COVERED
- The statistics of analytical methods
- Defining universal standards
- Making method operation uniform
- Training issues
- The use of Round-robin Samples.
- The Statistic of Transferring Methods
WHO WILL BENEFIT?
- Lab Chemists
- Lab Managers
- Lab Technicians
- Lab Analysts
- Industries into Compliance Methodology (Biotech, Pharma) Companies into Environmental Compliance or EPA
- The statistics of analytical methods
- Defining universal standards
- Making method operation uniform
- Training issues
- The use of Round-robin Samples.
- The Statistic of Transferring Methods
- Lab Chemists
- Lab Managers
- Lab Technicians
- Lab Analysts
- Industries into Compliance Methodology (Biotech, Pharma) Companies into Environmental Compliance or EPA
Speaker Profile
John Fetzer
John C. Fetzer has had over 30 years of experience in laboratory compliance, including developing methods, writing SOPs, training, and auditing. He has served on the editorial advisory boards of the Journal of Chromatography, Analytical Chemistry, and Analytical and Bioanalytical Chemistry.
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