A method of controlling a blood analyzer for measuring platelets is provided. The method comprises: determining a relationship between at least one first measurement value obtained by detecting platelets in at least one previous test by an electrical type detector of the blood analyzer and at least one second measurement value obtained by detecting the platelets in the at least one previous test by an optical type detector of the blood analyzer, and controlling the blood analyzer to prepare the first and/or second measurement sample for a current test according to the determined relationship.

A method of operating an analytical laboratory is presented. The method comprises recording time at which samples are first identified; retrieving an order list comprising test orders for the samples; retrieving a degradation limit to each test order; determining workflows for each sample; instructing the laboratory instruments to carry out the test orders according to the workflows. Determining the workflows comprises i) determining target instruments capable of carrying out the test orders; ii) determining a sequence/timing of the test orders; iii) calculating an estimated completion time for each test order; iv) determining a lead time for each sample and test order; v) prioritizing test orders if the lead time exceeds the degradation limit. Steps ii) to v) are repeated until the lead time doesn't exceed the degradation limit for any of the test orders; or until steps ii) to v) have been repeated for a number N of iterations.

Systems and methods are provided for sample processing. A device may be provided, capable of receiving the sample, and performing one or more of a sample preparation, sample assay, and detection step. The device may be capable of performing multiple assays. The device may comprise one or more modules that may be capable of performing one or more of a sample preparation, sample assay, and detection step. The device may be capable of performing the steps using a small volume of sample.

In order to easily identify a specimen to be extracted because, for example, an item remains uninspected, from a rack 31 collected in a storage part 13 or the rack 31 taken out from the storage part, a camera of a smart device takes an image of the rack; and a calculation unit included in the smart device provides a mark, by AR technology, at the position of a specimen to be extracted. For example, the item that remains uninspected is identified on the basis of information about a combination of a rack ID and an identifier and information, which is received from an operation unit about specimens at respective positions. Thus, irrespective of a place or whether the specimen to be extracted is inside or outside of the device, the specimen to be extracted can be reliably specified from a plurality of specimen containers provided on a holder.

In medical analysis devices and automatic specimen examination systems, the specimen conveyance mechanism is constituted by a plurality of belt lines. During installation or maintenance of the specimen conveyance mechanism, it is necessary to confirm the existence of steps at the joints of these belt lines and the parallelism of the conveyance line. According to the present invention, it is possible to lighten the burden of this work with a test tube type or conveyance holder type inspection device provided with a sensor and battery for operation. Also, even when an operator cannot visually confirm the conveyance line from outside, it is possible to confirm the state of the conveyance line.

Provided is an automatic analyzer that has a plurality of mechanisms including a mechanism that suctions reaction waste liquid and a mechanism that suctions cleaning liquid, etc. on a sample and a probe surface, the automatic analyzer reducing pressure in a vacuum tank using a pressure-reducing pump, etc., and suctioning waste liquid by negative pressure in the vacuum tank. A contact point of a vacuum switch that is provided in the vacuum tank is closed when the pressure in the vacuum tank reaches a specified negative pressure, and then the analyzer becomes ready for analysis. If any flow path portion of any mechanism that connects with the vacuum tank becomes clogged, suctioning operation cannot be performed properly and analysis performance is affected. The vacuum pump is switched off at a timing at which each solenoid valve connecting to the vacuum pump is individually opened, and the time that elapses before the pressure in the vacuum tank reaches the specified negative pressure is measured. The measured time is compared with parameters in a normal case, and the presence or absence of an anomaly is determined.

Disclosed is a specimen analyzer configured to perform analysis on a specimen for a plurality of measurement items, the specimen analyzer including a measurement section configured to perform a specimen measurement for measuring a measurement sample prepared from a specimen and a reagent corresponding to a measurement item, and configured to perform a quality control measurement for measuring a measurement sample prepared from a quality control substance and a reagent corresponding to a measurement item; and a controller programmed to set a quality control for each measurement item, from a quality control group that includes at least two types of quality controls selected from a first quality control in which the quality control measurement is performed at a predetermined time, a second quality control in which the quality control measurement is performed every time the specimen measurement is performed a predetermined number of times of measurement, and a third quality control in which the quality control measurement is performed every predetermined time interval, the controller being programmed to control the measurement section in accordance with the set quality control.

Systems and methods are provided for sample processing. A device may be provided, capable of receiving the sample, and performing one or more of a sample preparation, sample assay, and detection step. The device may be capable of performing multiple assays. The device may comprise one or more modules that may be capable of performing one or more of a sample preparation, sample assay, and detection step. The device may be capable of performing the steps using a small volume of sample.

To reduce the risk of mistaken operation and improve convenience in an automatic analysis device. Information about types of measurement inputted from an input device is combined in an examination mode creation screen image 301 on a display device of an automatic analysis device that performs analysis of specific types of measurement on a specimen container accommodating a specimen, the information about types of measurement including biochemistry examination items 303, immunology examination items 304, ISE examination items 304, blood clotting examination items 306, etc. This information is associated with an examination mode name 302, which comprises discretionary setting information, and is stored in a table of a storage unit. Information which is to be displayed on the display device and for which a change in settings is to be enabled is limited on the basis of the stored information about types of measurement associated with the examination mode name 302.

Carriers are provided for microbiological laboratory use, as are methods for their use. The carriers may be used to transport patient samples between laboratory stations and can be loaded into automated AST systems. In an aspect, a method of performing AST may include loading a tube comprising a patient sample onto a carrier. An AST panel may be loaded onto the carrier. The carrier may be conveyed to an automated inoculation assembly. The patient sample may be inoculated from the tube into the AST panel. The AST panel may be loaded into an automated AST system.