In bioprocessing, thorough cleaning is critical in order to take full benefit of the resin by removing impurities. When using conventional chromatography solutions, cleaning and cleaning validation consumes a considerable amount of time and facility resources. Cleaning-in-place protocols are performed before, during, and after a campaign.
A major bottleneck is the time it takes to get the results from the cleaning verification process. This problem can be addressed by using single-use technologies, which eliminate the need for cleaning and cleaning validation.
To learn more about downstream single-use opportunities and other ways to gain efficiency in downstream bioprocesses, download the white paper: Unlocking the Potential for Efficiency in Downstream Bioprocesses.