Systems And Methods For Infusion Pump Formulary Validation

Non-transitory computer readable storage media storing instructions that when executed by at least one processor cause the at least one processor to perform operations comprising:

• generating validation infusion pump instructions for a first infusion pump corresponding to an infusion pump operational instruction configuration and a plurality of test combinations of at least an infusible material, a dosage, and a synthesized subject, wherein the plurality of test combinations are generated from a set of configuration files defining at least a plurality of infusible materials, a plurality of dosages, and a plurality of synthesized subjects;
• pushing the validation infusion pump instructions to the first infusion pump causing the first infusion pump to perform infusions in accordance with executing each instruction from the validation infusion pump instructions;
• monitoring output signals of the first infusion pump during execution of the validation infusion pump instructions by the first infusion pump;
• and
• populating a validation file with the output signals of the first infusion pump.

A system for infusion pump validation, the system comprising:

• at least one first infusion pump configured to execute operational instructions having a first configuration;
• at least one second infusion pump configured to execute with operational instructions having a second configuration;
• at least one processor;
• and
• non-transitory computer readable media storing instructions that when executed by the at least one processor cause the at least one processor to perform operations including:
• generating a first validation infusion pump operational instruction set for the at least one first infusion pump using the first configuration of the operational instructions associated with the at least one first infusion pump and a first plurality of test combinations of at least an infusible material, a dosage, and an infusion rate for a synthesized subject;
• generating a second validation infusion pump operational instruction set for the at least one second infusion pump using the second configuration of the operational instructions associated with the at least one second infusion pump and a second plurality of test combinations of at least an infusible material, a dosage, and a dosage rate for a synthesized subject;
• pushing the first validation infusion pump operational instruction set to the at least one first infusion pump causing the at least one first infusion pump to operate in accordance with executing first validation instructions from the first validation infusion pump operational instruction set;
• pushing the second validation infusion pump operational instruction set to the at least one second infusion pump;
• monitoring first output signals of the at least one first infusion pump during execution of the first validation instructions by the at least one first infusion pump;
• monitoring second output signals of the at least one second infusion pump during execution of the second validation infusion pump operational instruction set by the at least one second infusion pump;
• and
• populating a validation file with the first output signals of the at least one first infusion pump and the second output signals of the at least one second infusion pump.