Work, such as status confirmation, in a plurality of automatic analyzers is efficiently performed. In an automated analysis system, a tablet terminal 114 has a terminal information management unit 210 and a terminal display unit 208. A terminal information management unit 210 acquires device information showing the state status of a device from automatic analyzers 101a to 101d, and generates a status confirmation screen showing the device status of the automatic analyzer. A terminal display unit 208 displays the status confirmation screen. The status confirmation screen has a status information screen showing the device status of one automatic analyzer and a device switch button configured to switch the status information screen to a status information screen corresponding to another other automatic analyzer. When the switch button is selected, the terminal information management unit 210 generates a status confirmation screen for an automatic analyzer corresponding to the selected switch button, and displays the status confirmation screen on the display unit.

The present invention covers the integration and utility of accelerometer features into a clinical analysis system. For example, measurement of dynamic acceleration and orientation of a blood-testing instrument with respect to Earth's gravitational field may be used to determine reliability of a test procedure and optionally to provide corrective elements thereof.

Provided is an automatic analyzer in which a consumable is appropriately managed and efficiently used.

An automatic analyzer includes: a housing container holder portion that holds a housing container housing a consumable; a transport mechanism that transports the consumable housed in the housing container; and a controller, in which the housing container contains a first consumable and a second consumable, and the controller determines a usage state of the housing container relating to the first consumable and a usage state of the housing container relating to the second consumable, determines whether or not the first consumable housed in the housing container is usable based on the usage state of the housing container relating to the first consumable, and determines whether or not the second consumable housed in the housing container is usable based on the usage state of the housing container relating to the second consumable.

A method to provide control samples for validating a diagnostic test within a laboratory system is presented. The laboratory system comprises an aliquoting device, a storage, a transport system, at least two analyzers, and a control unit. A total number of control sample aliquots and an aliquot volume for each control sample aliquot is determined based on a validation time schedule. A provided total control sample volume is aliquoted into the determined total number of control sample aliquots with the determined aliquot volumes. The generated control sample aliquots are transported to one or more of the at least two analyzers according to the validation time schedule.

A method for preparing a deck for a process is disclosed. The deck can be prepared with any necessary components, and then an imaging device can capture an image of the deck. This image can be compared with a reference image and any differences identified. The differences can be indicated in the image and shown to an operator, such that the operator can correct any errors associated with the differences.

An analyzing apparatus is disclosed that is capable of preventing an intentional or negligent interventional action on an analysis. An analyzing apparatus 1 is connected to a controlling computer 2 and performs a predetermined analysis according to a control instruction given through the controlling computer 2. The analyzing apparatus 1 includes an operation unit 11 for enabling a user to perform an input operation for controlling the analyzing apparatus 1. When the analyzing apparatus 1 is under control of the controlling computer 2, the input operation performed through the operation unit 11 is disabled.

A sensor device includes a sensor array and a flow cell in fluid communication with the sensor array. Bias circuitry apply bias arrangements to the sensor array to produce sensor data. Peripheral circuitry coupled to the bias circuitry produces streams of data from the sensor array, the peripheral circuitry having an active mode and an idle mode. Logic to switch the peripheral circuitry between the active mode and the idle mode to control power consumption is provided. A temperature sensor may be included, and the logic can operate with feedback to switch between the active mode and the idle mode to maintain the temperature within an operating range.

The present invention makes it possible for an automated analyzer including two or more types of photometers to obtain suitable output of the measurement results of the plurality of photometers and suitable data alarm output even if there is an abnormality, or the like, at the time of measurement. This automated analyzer includes, for example, two types of photometers having different quantitative ranges and an analysis control unit for controlling analysis that includes measurement of a given sample using the two types of photometers. If two types of data alarms corresponding to abnormalities, or the like, during measurement have been added to the two types of measurement results from the two types of photometers, the analysis control unit selects measurement result and data alarm output corresponding to the combination of the two types of data alarms and outputs the same to a user as analysis results.

An automatic analysis device includes a probe that performs a dispensing operation including a suction process and a discharge process with respect to liquid; a syringe that generates a pressure change for dispensing liquid at the probe; a flow path that connects the probe and the syringe with each other; a pressure sensor that measures the pressure change in the flow path at the time of liquid dispensing; a storage portion that stores a pressure change of time-series when reference fluid is discharged as a reference discharge pressure waveform; and a determination portion that determines whether or not there is an abnormality in the suction process of the sample from a relationship between a value of difference or a ratio between the reference discharge pressure waveform and the pressure waveform of a determination target at the time of discharge of liquid and normal range.

The present disclosure provides a system and methods for qualifying a diagnostic apparatus and/or a reagent used by the diagnostic apparatus. Also disclosed are programs therefor.