Description: Automation liberates scientists from spending all their time on routine tasks leaving them to spend more time on science. In the past, automation has been challenging to implement – particularly for regulated labs attempting to transfer assays from a nonregulated lab. Prior automation solutions were also limited by cartridge capacity, but not anymore. In this session, we will discuss how combining precision liquid flow control, microchromatography cartridges with diverse resin chemistries, and intuitive software brings the power of chromatography to sample preparation. This solution is tailored to address the wide variety of protein sample preparation workflows used in proteomics and biotherapeutic drug discovery and development. Optional compliance enabling features, including permission level controls, allows walkup operation and seamless transfer of assays between noncompliant and compliant labs. New, larger bed volume cartridges provide the capacity necessary to address the critical quality attributes required for large molecule biotherapeutics.
Learning Objectives:
Discover how the process makes automated sample preparation accessible to non-automation experts to reduce variability, human error and manual labor.
Learn how new 21 CFR part 11 enabling features in the software allows for walkup operation and simplify transfer of assays along the entire biotherapeutic development process.
See the workflows that are enabled with the large capacity cartridges.
