Provided are a device and a method capable of determining an optimal retrieving condition of a specimen rack according to various situations, when an error occurs in any specimen among a plurality of specimens mounted on the specimen rack. When the error occurs in a specimen accommodated in a specimen container mounted on the specimen rack, conveyance of the specimen rack is controlled on the basis of information about the specimen having the error and a specimen accommodated in another specimen container on the specimen rack on which the specimen container with the specimen accommodated therein is mounted, and the retrieval condition of the specimen rack.

In a case where plural measurement items that require different incubation times are simultaneously measured in an automatic analyzer, deterioration of the turnaround time of the measurement is minimized. The automatic analyzer receives a request of a sample, obtains a ratio of a short measurement item among examination items of the received analysis request, and a determines an empty cycle based on the ratio of the short measurement item and the number of schedules. When an empty cycle is necessary, the empty cycle is scheduled in a schedule of a sample that is requested to be measured first, for example, an empty cycle in a short measurement for making an incubator empty. As a result, this position can be used for a measurement of a short measurement item such that the wait time of the start of the measurement can be short.

An automatic analyzer includes: a reagent mounting unit 103 in which a plurality of reagent bottles 10 are installed when a reagent bottle 10 is loaded into the automatic analyzer; a reagent conveying mechanism 101 including a gripper mechanism 106; and a reagent mounting mechanism 102 for moving the reagent mounting unit 103 between an installation position at which an operator installs the reagent bottle 10 in the reagent mounting unit 103 and a position at which the gripper mechanism 106 grips the reagent bottle 10. It is thereby possible to achieve saving of a mechanism installation space and reduction of the number of constituent components, automatically carry out an operation from opening of the reagent bottle to loading of the reagent bottle into the reagent disk, and alleviate an operator's burden.

Embodiments of the present disclosure relate to a method, system and apparatus for setting a clotting time for a blood sample contained in a container in a laboratory device or test system, which includes setting a clotting start time for the blood sample, setting a clotting wait time to allow for the blood sample to clot, and on positive determination of the completion of the clotting wait time, automatically providing the blood sample for further processing in the laboratory.

There is provided an electrolyte analyzer that can appropriately replace consumable items while more exerting analysis processing performances than a conventional electrolyte analyzer does. An electrolyte analyzer includes a plurality of analysis chambers 50 having ISE electrodes 1 configured to measure the concentration of the electrolyte of a sample and a controller 29 configured to control operations in the electrolyte analyzer 100 including the analysis chambers 50. The ISE electrodes 1 of the plurality of analysis chambers 50 analyze the same analysis items. The controller 29 selects an analysis chamber 50 used for measurement from the plurality of analysis chambers 50 corresponding to the remaining measurable numbers of a plurality of ISE electrodes 1 and measurement request status.

An automatic sample injection device is configured to perform an injection operation of a sample to an analyzer by a sampling mechanism (2) for sucking and dispensing a solvent. The automatic sample injection device is provided with solvent arrangement locations (14) at which a plurality of solvents each accommodated in a vial is arranged, a method setting unit (16) configured to set a method of a predetermined operation using a solvent based on information input by a user, a solvent arrangement setting unit (20) configured to set the number or types of solvents to be arranged at the solvent arrangement locations; and a control unit (6) configured to control the sampling mechanism to execute the predetermined operation with a method set by the method setting unit.

Provided is an automatic analyzer which does not require a preparation operation of disposing of a reaction vessel on the apparatus in advance and is capable of efficiently performing shifting to an analysis operation.

In a reaction promotion unit 108, a holding position located at a reaction vessel disposal position 202 during a first operation cycle is moved to a reaction vessel setting position 201 after an n (n: integer) operation cycle, and from a first operation cycle to an n-th operation cycle, an expendable item transport unit 112 performs an operation of disposing of a reaction vessel from a disposal position without performing an operation of setting the reaction vessel at a setting position in each operation cycle, and performs an operation of setting the reaction vessel at the setting position and an operation of disposing of the reaction vessel from the disposal position in each operation cycle after an (n+1)-th operation cycle.

In a risk level assessment method for a plurality of clinical conditions as follows, a set of laboratory test results (32) are stored with time stamps for a patient, including at least one hematology test result and at least one arterial blood gas (ABG) test result. For each clinical condition, a risk level is determined for the clinical condition based on a clinical condition-specific sub-set of the stored set of laboratory test results. This determination is made conditional on the stored clinical condition-specific sub-set of laboratory test results being sufficient to determine the risk level. A time stamp is assigned to each determined risk level based on the time stamps for the laboratory test results of the clinical condition-specific sub-set of laboratory test results. A display device (44, 46) displays the determined risk level and the assigned time stamp for each clinical condition whose determined risk level satisfies a display criterion.

A server stores a set of laboratory applications to process batches of samples. The server receives, from a first lab administrator, a selection of a subset of the laboratory applications to process the batches of samples and an admin configuration for a laboratory application in the subset. The server receives configuration(s) of batch(es) to be used for running at least a portion of the subset of laboratory applications configured according to the admin configuration. The server receives, from a first scientific device, a request to run a laboratory application form the first subset to process a batch. The server provides the laboratory application(s) that are capable of being executed using the first scientific device. The server receives, from the first scientific device, a selected laboratory application. The server transmits, to the first scientific device, a signal for executing a first part of the selected laboratory application.

An optimization method of a diagnostic laboratory system. The method includes receiving, at a system controller, computer-readable data comprising an inventory of a plurality of analyzers included within the diagnostic laboratory system, and types of tests and numbers of the tests to be performed on samples by the diagnostic laboratory system over a planning period; and determining, via a reagent pack optimization module executing on the system controller, a reagent pack loading plan over the planning period. Diagnostic laboratory systems are disclosed, as are other aspects.