In this webinar, we will discuss how the combination of next-generation SPE technology and solid core LC columns delivers improved efficiency to regulated bioanalytical workflows. It will be demonstrated that the combination provides higher levels of cleanliness, reproducibility, throughput, sensitivity and quality of results, with lower failure rates.
Using an analysis designed to meet the requirements of the EMEA Guidelines on bioanalytical method validation we will investigate the workflow improvements that these sample preparation and liquid chromatography techniques offer: showing comparisons with competing technologies.
Key Learning Objectives
How the latest sample preparation and LC column technologies can improve:
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Quality of results
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Efficiency and output of the bioanalytical laboratory
How these improvements can be achieved while:
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Maintaining ease-of-use and current platforms
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Complying fully with current method validation guidelines
Who Should Attend
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Bioanalytical group heads
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Bioanalytical laboratory managers
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Bioanalytical method developers
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Bioanalytical laboratory technicians
Presenters
Mike Oliver
Product Manager
Sample Preparation,
Chromatography Consumables
Thermo Fisher Scientific
Stephen Luke
Product Manager
Liquid Chromatography,
Chromatography Consumables
Thermo Fisher Scientific