Analytical chemistry techniques based on separation science are critical in the analysis of pharmaceuticals and biopharmaceuticals. In chromatography and electrophoresis, integration is the process of determining the area of a peak and thus enabling quantitative analysis. The control of the integration process is extremely important, particularly in a GMP environment, because it determines the quality of the final results generated, and it can be manipulated to falsify data. Therefore, we need to be able to demonstrate that there is no risk to data integrity.
On this course, you will learn about the integration algorithms in common integration software packages and the functions of the parameters involved, so that you can ensure, and demonstrate, that the integration has been applied in the most appropriate manner.
This course is suitable for anyone who integrates chromatography or reviews the data generated from integration processes. For example:
On this course, you will learn about the integration algorithms in common integration software packages and the functions of the parameters involved, so that you can ensure, and demonstrate, that the integration has been applied in the most appropriate manner.
Learning Objectives
- Understand the key concepts of how integration is applied,
- Be able to process chromatography using available integration parameters, and
- Be able to find the best solutions for issues associated with difficult chromatography, such as poorly resolved peaks.
Delivery
This half day 鈥榲irtual鈥� live online training event is delivered over a 3 hours and 45 minutes period, from 12pm to 3:45pm, including a short break. The time zone is BST (GMT+1).This course is suitable for anyone who integrates chromatography or reviews the data generated from integration processes. For example:
- Development and Quality Control (QC) analytical chemists
- Reviewers in development and Quality Control (QC)
