The US Food and Drug Administration (FDA) / Center for Biologics Evaluation and Research (CBER), requires brand name or equal Automatic Helium Purifier to improve efficiency of liquid helium production and reduce to a minimum human intervention to keep the HRS working. The instrument shall be integrated seamlessly as a component of our HRS from the moment it arrives. This incorporation will allow unsupervised helium liquid production for long periods of times with higher reliability than we currently achieve.