One variation of a method includes, during a calibration period: triggering collection of an initial bioaerosol sample by an air sampler located in an environment; and triggering dispensation of a tracer test load by a dispenser located in the environment; accessing a detected barcode level of a barcode detected in the initial bioaerosol sample; accessing a true barcode level of the barcode contained in the tracer test load; and deriving a calibration factor for the environment based on a difference between the detected barcode level and the true barcode level. The method further includes, during a live period succeeding the calibration period: triggering collection of a first bioaerosol sample by the air sampler; accessing a detected pathogen level of a pathogen detected in the first bioaerosol sample; and interpreting a predicted pathogen level of the pathogen in the environment based on the detected pathogen level and the calibration factor.

An in-vitro diagnostic analyzer, a reagent card (10), and an installation structure (200) are disclosed. The installation structure (200) includes an installation body (210). The installation body (210) includes an installation hole (212) configured to sleeve a sample tube (70), a hollow needle (220), a sealing portion (240), and an air inlet channel (230). One end of the hollow needle (220) is capable of being inserted into the sample tube (70). The sealing portion (240) is in sealing fit with an outer wall of the sample tube (70). The air inlet channel (230) includes an air outlet hole (234) and an air inlet hole (232). The air outlet hole (234) is configured for communication with the sample tube (70) provided on the installation hole (212). The reagent card (10) is integrated with the installation structure (200), and the in-vitro diagnostic analyzer is integrated with the reagent card (10).

Techniques and apparatus for evaluating analytical device performance and data quality are described. In one embodiment, for example, an apparatus may include at least one memory, and logic coupled to the at least one memory. The logic may be configured to generate an analysis method to be performed by an analytical device, the analysis method comprising a plurality of method segments comprising at least one performance assessment process and at least one sample analysis process, and link the at least one performance assessment process with the at least one sample analysis process. Other embodiments are described.

An automatic analyzer includes a control unit 7d that, when an accuracy control sample is put in after input of a standard sample, requests measurement of the input accuracy control sample on the same measurement item as a requested measurement item for the standard sample; and a selection screen 201 or 501 that enables selection of measurement timing of the accuracy control sample on the same item as the requested measurement item for the standard sample. The control unit 7d starts measurement of the accuracy control sample when the timing selected on the selection screen 201 or 501 is reached. This reduces consumption of the standard sample and reagent as compared with before and provides an automatic analyzer that can improve analysis throughput.

Provided is an automatic analysis device in which a step for checking the progress of deterioration of a reagent can be automated and the expiration date of the reagent can be managed. Properties in absorption spectroscopic analysis pertaining to a standard liquid during implementation of calibration are used to calibrate the automatic analysis device so as to generate a standard curve N times for each lot. A series of action are repeated, with successive results in the implementation of calibration being updated while N is increased by 1 for each instance, until a first lot is completed. The final results are displayed in a dedicated screen image. This makes it possible to preliminarily ascertain the deterioration of the reagent, therefore making it possible to preemptively prevent inferiority in terms of repeatability and linearity, as well as to contribute to freedom from complex operations, reduction of cost, improvement in quality of data, and prevention of medical malpractice caused by a delay in reporting.

An automatic analyzing apparatus according to an embodiment includes first and second conveyance paths, a sample dispensing mechanism, and processing circuitry. The first conveyance path conveys a first container rack that holds a container housing the sample. The second conveyance path conveys a second container rack that holds a container housing at least one of a detergent solution for cleaning a probe that dispenses the sample, a diluent for diluting the sample, a buffer solution for mixing the sample, a solution used for a blank test with the sample, and a solution for performing calibration measurement for the apparatus. The sample dispensing mechanism is configured so that the probe can aspirate a liquid in the container of the first container rack and the second container rack. The processing circuitry controls operations of the first conveyance path, the second conveyance path, and the sample dispensing mechanism.

Described herein are methods and systems for the determination of constituents in biosamples by NMR spectroscopy and more specifically for the determination of lipoprotein constituents LP-X, LP-Y, and LP-Z in blood plasma and serum.

Provided is an automatic analysis device that shortens the confirmation time for calibration or precision management. This automatic analysis system includes an analysis device configured to perform an analysis for deriving a property of a specimen on the basis of the relative relationship between a measured value of a standard specimen for which the property is known and a measured value of the specimen, and a display device that displays information about calibration or precision management carried out on the analysis device using the standard specimen, the system being characterized in that the display device displays: a request list including request information about request for the calibration and/or the precision management; and/or a preparation list that displays, in an empty manner, a field of the standard specimen that corresponds to an in-rack position number where the standard sample is not to be placed, as preparation information about preparation of the standard specimen to be used, in accordance with the request, in the calibration and/or the precision management.

A system and method for calibration of analytical instruments includes a software application allowing users to compute, construct, display, review, select and evaluate initial calibration models. The software application summarizes the initial calibration using the method evaluation parameters and the user selected evaluation criteria in the initial calibration evaluation table. The software application is a mathematically based program that will independently compute, construct, and display the initial calibration for each target analyte. This program then uses logic functions to review and select calibration variables against evaluation parameters. The software application is a user friendly tool performing all of the calculations independent of the on-boarded software and displays that information on a novel data visualization platform. The software application is the answer to questions centering around software limitations users encounter with on-board instrument software.

Provided is an automatic analysis device that estimates causes of change in measurement values of a quality-control substance. An automatic analysis device that analyzes specimens includes an acquisition unit that acquires amount of change in measurement values of a quality-control substance used for quality control, a calculation unit that calculates a change prediction amount on the basis of a difference value in concentration values of a standard solution used for calibration before and after changing lots, and an estimation unit that estimates causes of change occurring in measurement values of the quality-control substance on the basis of results of comparing the amount of change and the change prediction amount.