Major efforts have been made in the last few years to enable faster chromatography runs, mainly through the use of UHPLC. Today many labs are performing 30 minute runs in only 3 minutes. However, the speed of data processing has often failed to keep up with the speed of analysis. Typical bottlenecks have been
- Amount of time required to generate sequences according to SOP
- Integration and calibration of data
- Calculating results
- Time to do all the above in compliance with the regulations, such as GxP and 21 CFR Part 11
In this webinar you will learn about these factors in the context of 2 typical analytical techniques – method validation and related substances testing. New software tools that will make these techniques less error-prone and time consuming, and reduce costs, increase throughput, and enhance productivity will be discussed.
This webinar will be of interest to anyone working in a pharmaceutical QA/QC lab, or interested in how to use chromatography software to solve day-to-day challenges in the analytical lab.
