Register Free at www.pharmtech.com/unique
Event Overview:
When validating a method according to the ICH guidelines, it is necessary to perform a linearity experiment. This requires the preparation of multiple calibration levels, analysis of the samples by liquid chromatography, and calculation/ reporting of the results. Each of these steps can be very time consuming, and in many cases error prone. This is especially true if the analytical method being tested requires the measurement of multiple components.
In this webinar we will present a new way to tackle these challenges. The webinar will demonstrate an automated approach to sample preparation, the use of UHPLC to speed-up the analysis, and the use of advanced software tools for calculation and reporting of the results. When used in combination, these tools substantially shorten the linearity workflow, and significantly reduce error rate.
Key Learning Objectives:
- Learn how automated sample preparation can save time and reduce error
- Learn how UHPLC can reduce sample analysis time by a factor of 5 or more
- Learn how a chromatography data system can fully automate calculation of the results
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Who Should Attend: |
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Anyone who has to manually prepare samples and standards |
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Anyone who works in pharma method development and QA/QC |
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Anyone who wants to see how UHPLC can improve productivity in their lab |
Speakers: |
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Joanne Ratcliff, PhD
Marketing Project Manager
Mettler-Toledo |
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Fraser McLeod
Senior Director of Product Marketing Dionex Corporation |
Sponsors: |
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