The Transfer Of Validated Methods
John C. Fetzer, has had over 30 year experience in HPLC methods development. He has authored or co-authored over 50 peer-reviewed papers on liquid chromatography, has served on the editorial advisory boards of the Journal of Chromatography, Analytical Chemistry, and Analytical and Bioanalytical Chemistry.
Even a detailed and well-written standard operating procedure for a method cannot ensure that 2 laboratories running on aliquots of the same will get statistically equivalent results. Using different instrumentation, standards, reagents, solvents, and other chemicals, data systems, sample storage and handling procedures, and other variables are common and can lead to different results. Making each operation as similar as possible can be time-consuming and complicated.
Areas 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 Should Attend
- Lab Chemists
- Lab Managers
- Lab Technicians
- Lab Analysts
- Industries into Compliance Methodology (Biotech, Pharma)
Why Should You Attend
Many methodologies are used in more than 1 facility. A common practice is that a method is developed at an R&D laboratory and then transferred to operating facilities for use. It is well known that there can often be no relationships between neither accuracy or 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.
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$200.00
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