| abstract |
The fluid delivery system may include a vessel containing a medical fluid, a fluid pressurization unit, and a fluid delivery set to deliver the medical fluid from the vessel toward the fluid pressurization unit. In order to verify the integrity and asepticity of the fluid delivery system, the system will follow an experimental protocol to assess the sensitivity of the system to pathogen entry, chemical degradation, and / or fluid cross contamination during the patient fluid delivery process. The experimental protocol can help ensure that the delivery system components used during a number of different fluid delivery processes are executed as well as ensuring that these components have been replaced after each fluid delivery process. |