An automated method of calibrating a sensor located in a flow-through sensor path and requiring at least one oxygenated calibration fluid for calibration comprises transporting a predefined amount of deoxygenated calibration fluid from a fluid supply into a fluidic line between a fluid-selection valve and the sensor path, transporting ambient air into the fluidic line before and after transporting the calibration fluid forming an isolated plug of calibration fluid between zones of ambient air, oscillating the calibration fluid plug back and forth within a predefined length of the fluidic line causing reciprocating fluid film tailing along the inner walls of the fluidic line, and facilitating oxygenation of the calibration fluid via oxygen uptake by the fluid film from the ambient air in the fluidic line, and transporting the oxygenated calibration fluid into the sensor path at a position where the sensor is located and calibrating the sensor.

A method of producing a sample collection apparatus, including steps of: attaching a holding member to a support of a nozzle unit such that, in slits provided with N edges (N≥3), a collection range w of a sample tube is included within a range from a lower-limit position at a distance w/2 from a 1st edge toward an initial-position, to an upper-limit position at a distance w/2 from an Nth edge away from the initial position; loading the sample tube on the holding member; counting the number of pulses with which a pulse motor is driven to move a nozzle to the center of the collection range; identifying the signal corresponding to the last edge recognized by a photo-interrupter before the nozzle reaches the center of the collection range; and storing the number of pulses and the signal corresponding to the last edge in a storage device.

Methods and systems for determining a dose of an analyte in an unknown sample on an instrument, such as a nucleic acid analyzer, immunoassay analyzer, or clinical chemistry analyzer using a reagent from a selected assay lot are described. The methods and systems use core dose-response information based on measurements of response values to a set of calibrators on a plurality of other instruments and assay lot-specific response information to calibrate the instrument.

An automatic analysis device is provided with: a sample disk for holding a sample container that accommodates a sample; a reagent disk for holding a reagent container that accommodates a reagent; at least two different measuring units that respectively perform different types of analyses; a control part that controls the measuring units; and a display part that displays: a work flow area in which the flow of operation of the two or more measuring units is displayed; and an overview area in which the usable or unusable states of the respective measuring units are displayed, wherein the overview area has a unit necessity-of-use selection part that can select whether using each of the measuring units is necessary, and the control part controls the display part so as to change the display of the work flow area on the basis of the information set in the unit necessity-of-use selection part.

A blood coagulation analyzing method according to one or more aspects may include: calculating a coagulation time based on data representing a coagulation curve of a change in an optical detection value of a blood specimen added with a reagent for starting a coagulation reaction; calculating an index value related to derivatives calculated concerning the coagulation curve represented by the data used in the calculating the coagulation time; and determining whether an early reaction error has occurred based on a comparison result obtained by comparing the index value to a predetermined threshold.

The present disclosure relates to a capsule for preparing a solution for use with a measuring device for determining a measurand that depends on a concentration of at least one analyte in a sample. The capsule includes a wall completely enclosing an interior, at least one substance accommodated within the interior, and at least one stirring body. The present disclosure also relates to a system, which includes at least one capsule and a liquid container closed in a liquid-tight manner, which contains a predetermined volume of a liquid containing a solvent. In addition, the wall of the capsule is formed from a material which dissolves at least partially in the solvent.

Systems and methods are described to determine a prioritization schedule for samples handled by a system with multiple remote sampling systems. A system embodiment includes, but is not limited to, an analysis system at a first location; one or more remote sampling systems at remote from the first location, the one or more remote sampling systems configured to receive a liquid segment and transfer a liquid sample to the analysis system via a transfer line; and a controller communicatively coupled with the analysis system and the one or more remote sampling systems, the controller configured to assign a priority value to a sample for analysis by the analysis system and to manage a queue of samples received from at the one or more remote sampling systems on the basis of the assigned priority value.

Various embodiments include an exemplary apparatus and method for insitu calibration of multiple flow-sensing devices within a dilution system. In one example, a calibration and dilution system includes a first mass-flow device to serve as a global reference, a second mass-flow device configured to be coupled to and provide a supply of clean gas to a primary diluter, and a third mass-flow device configured to be coupled to and provide a supply of clean gas to a secondary diluter, where the diluters are pneumatically coupled to one another through a gas-supply line. Multiple valves are coupled to at least the mass-flow devices and the diluters. The calibration and dilution system is arranged so that the mass-flow controllers can be calibrated in-situ without having to remove any of the mass-flow controllers from the calibration and dilution system. Other apparatuses, designs, and methods are disclosed.

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.

A quality check module for characterizing a specimen and/or a specimen container including stray light compensation. The quality check module includes an imaging location within the quality check module configured to receive a specimen container containing a specimen, one or more image capture devices configured to capture images of the imaging location from one or more viewpoints, and one or more light sources configured to provide back lighting for the one or more image capture devices, and one or more stray light patches located in an area receiving stray light from the one or more light sources enabling stray light affecting the images to be compensated for and to provide a stray light compensated image. Calibration methods, methods of characterizing a specimen, specimen testing apparatus including a quality check module, and specimen container carriers including one or more stray light patches are provided, as are other aspects.