A maintenance method in an automatic analysis apparatus includes: a recognition step of recognizing an integrated rack 301A, 301B, 301C mounted with a cleaning solution container containing a cleaning solution, and a calibrator container containing a calibrator or a QC specimen container containing a QC specimen containing a sample having a known concentration; a cleaning solution supply step of aspirating a cleaning solution; and a supply step of aspirating the calibrator or aspirating the QC specimen, in which the cleaning solution supply step and the supply step are continuously performed from the cleaning solution container and the calibrator container or the QC specimen container mounted on the integrated rack 301A, 301B, 301C. Accordingly, an automatic analysis apparatus and a maintenance method in the automatic analysis apparatus that can reduce a burden on a user in calibration and the like during maintenance are provided.

A method to make it possible to obtain a value related to the amount of DD by FDP measurement. The method includes optically measuring a first calibration sample prepared from an FDP measurement reagent and a first calibrator containing D-dimer (DD) and having a first value relating to the ratio of the content of fibrin/fibrinogen degradation product FDP to the content of DD, acquiring first calculation data based on temporal change of optical information obtained by optical measurement of the first calibration measurement sample, performing optical measurement of a second calibration measurement sample prepared from FDP measurement reagent and a second calibrator containing DD and having a second value that is different from the first value related to the ratio of the content of FDP to the content of DD, acquiring second calculated data based on a temporal change in optical information obtained by optical measurement of the second calibration measurement sample, and acquiring calibration curve information indicating the relationship between the calculation data and the value relating to the amount of DD based on the first calculation data, the second calculation data, the first value, and the second value.

The present invention provides a capping system for biological thermal reaction, which comprises at least one reaction tube, at least one suction unit, and at least one pushing rod. Each of the at least one reaction tube comprises an opening end. The at least one suction unit is used to suck at least one cap and move the at least one cap to the opening end of the at least one reaction tube. The at least one pushing rob is used to push the at least one cap into the opening end of the at least one reaction tube.

Provided is an analysis device capable of reducing vibration and noise generated by a stepping motor due to countermeasure for step-out of the stepping motor. A drive unit is controlled such that a set value of driving torque of the stepping motor increases stepwise in a plurality of steps each time the step-out of the stepping motor is detected by the step-out detection unit.

A quality control sample measurement method, a sample analysis device and a supply device capable of normally acquiring a measurement result of a quality control sample are provided. The quality control sample measurement method for measuring a quality control sample stored in a cold state includes a step of stirring the quality control sample in a first operation mode (step S2) and a step of measuring the stirred quality control samples (step S3). The stirring in the first operation mode differs from the stirring in the second operation mode for stirring the subject sample collected from the subject.

A method of operating a sensor system including at least one sensor for detecting an analyte gas and a control system includes electronically interrogating the sensor to determine the operational status thereof and upon determining that the operational status is non-conforming based upon one or more predetermined thresholds, the control system initiating an automated calibration of the sensor with the analyte gas or a simulant gas.

The disclosure concerns a method for operating an automated analyzer, including transporting a liquid containing a plurality of particles into a chamber, such as a reactor chamber and/or measuring cell chamber of the analyzer, introducing a gas or gas mixture, for example, air into the chamber, such as through the liquid present in the chamber so that the particles in the liquid are stirred up, and subsequently draining at least part of the liquid from the chamber through a fluid line ending in the chamber and an open valve arranged in the fluid line.

An automatic analyzer having no limitation on a range of a placeable position on a sample placement disk for patient specimens, emergency specimens, quality control samples, and calibration samples, and being capable of performing analysis while changing the number of simultaneously-measurable samples for each type of each specimen is provided. In the automatic analyzer, either a calibration sample dedicated disk or a patient specimen dedicated disk is placed in an analyzing unit 8 as a sample placement disk 19, and the analyzing unit 8 has a disk identifying unit 24 which identifies a type of the sample placement disk 19, and a computer 22 identifies the type of the sample placement disk 19 based on an identification result of the disk identifying unit 24, and performs analysis on a liquid sample based on the identified type of the sample placement disk 19.

A method to normalize at least one of a population of subordinate clinical diagnostic analyzer to a master clinical diagnostic analyzer such that an assay result from a subordinate clinical diagnostic analyzer can be converted to the equivalent result of the master clinical diagnostic analyzer by using a simple multiplicative factor when the assay executed on each analyzer uses a common fluorescently labeled dye. Also a method to re-normalize a subordinate clinical diagnostic analyzer assay result to a master clinical diagnostic analyzer assay result by using a simple multiplicative factor when the assay executed on the subordinate clinical diagnostic analyzer uses a different fluorescently labeled dye than the assay executed on the master clinical diagnostic analyzer.

An electrode cleaning and calibration system generally comprises a sensor holder assembly machined from a block of solid acrylic or similar plastic material, which can accommodate a variety of types and sizes of sensors for use in monitoring and measurement of water processing and treatment processes. Examples of sensors suitable for use in the system include pH sensors, dissolved oxygen sensors, chlorine sensors, ozone sensors, total suspended solid sensors, mixed liquor suspended solid sensors, ammonia sensors, monochloramine sensors, and ultraviolent transmittance sensors.