Abstract: Disclosed herein are glass pharmaceutical vials having sidewalls of reduced thickness. In embodiments, the glass pharmaceutical vial may include a glass body comprising a sidewall enclosing an interior volume. An outer diameter D of the glass body is equal to a diameter d1 of a glass vial of size X as defined by ISO 8362-1, wherein X is one of 2R, 3R, 4R, 6R, 8R, 10R, 15R, 20R, 25R, 30R, 50R, and 100R as defined by ISO 8362-1. However, the sidewall of the glass pharmaceutical vial comprises an average wall thickness Ti that is less than or equal to 0.85*s1, wherein s1 is a wall thickness of the glass vial of size X as defined by ISO 8362-1 and X is one of 2R, 3R, 4R, 6R, 8R, 10R, 15R, 20R, 25R, 30R, 50R, and 100R as defined by ISO 8362-1.

Abstract: Disclosed herein are glass pharmaceutical vials having sidewalls of reduced thickness. In embodiments, the glass pharmaceutical vial may include a glass body comprising a sidewall enclosing an interior volume. An outer diameter D of the glass body is equal to a diameter d1 of a glass vial of size X as defined by ISO 8362-1, wherein X is one of 2R, 3R, 4R, 6R, 8R, 10R, 15R, 20R, 25R, 30R, 50R, and 100R as defined by ISO 8362-1. However, the sidewall of the glass pharmaceutical vial comprises an average wall thickness Ti that is less than or equal to 0.85*s1, wherein s1 is a wall thickness of the glass vial of size X as defined by ISO 8362-1 and X is one of 2R, 3R, 4R, 6R, 8R, 10R, 15R, 20R, 25R, 30R, 50R, and 100R as defined by ISO 8362-1.

Abstract: Implementations are directed to improving healthcare services. In some aspects, a method includes receiving a plurality of requests for assessing quality of care, the plurality of requests for assessing quality of care including health data of a plurality of patients; training, a risk score machine learning (ML) model using the health data; receiving, from a user device, a request for assessing of quality of care for a particular patient, the request including the particular patient’s private health information; performing assessment of quality of care using the particular patient’s private health information; generating a risk score input from the particular patient’s private health information; generating risk scores for one or more potential health conditions for the particular patient by executing the risk score ML model using the risk score input; and providing i) the quality of care assessment result and ii) the risk scores for output on the user’s device.

Abstract: A method includes providing a plurality of simulation components (101-105), each simulating operation of a distinct element of a cyber-physical system and including at least first and second simulation components (101, 102) arranged in series with one or more outputs of the first simulation component (101) being provided as input to the second simulation component (102). A plurality of output predictions are generated using a surrogate model of the first simulation component and, in response, a plurality of the second simulation components (102-1, 102-2, 102-3), or a plurality of second surrogate models, are executed in parallel. The input values of each second simulation component (102-1, 102-2, 102-3), or surrogate model corresponds to a respective one of the plurality of output predictions from the surrogate model of the first simulation component (101).

Abstract: Systems and methods for automatically managing and increasing the efficiency of non-authorized software installation such as on mobile devices having restricted operating systems.

Abstract: In accordance with one aspect of the present disclose, a fluid compressor for compressing a fluid is disclosed. The fluid compressor has a frame and a piston assembly. The piston assembly has a compression chamber connected to the frame, and the compression chamber includes a movable piston inside of the compression chamber along with a connection rod of a smaller transverse dimension than the diameter of the piston connected to the piston at a first end of the connection rod. The fluid compressor further has a pivot point located on the frame, and a lever connected to the pivot point. The lever has a short end and a long end on opposite sides of the pivot point, and the short end is connected to a second end of the connection rod. Further included is a lifting device for raising and lowering the lever.

Abstract: A method and automated apparatus for rapid non-invasive detection of a microbial agent in a test sample is described herein. The apparatus may include one or more means for automated loading, automated transfer and/or automated unloading of a specimen container. The apparatus also includes a detection system for receiving a detection container, e.g., container or vial, containing a biological sample and culture media. The detection system may also include one or more heated sources, holding structures or racks, and/or a detection unit for monitoring and/or interrogating the specimen container to detect whether the container is positive for the presence of a microbial agent therein. In other embodiment, the automated instrument may include one or more, bar code readers, scanners, cameras, and/or weighing stations to aid in scanning, reading, imaging and weighing of specimen containers within the system.

Abstract: A multi-layered implant and methods of forming the multi-layered implant are disclosed. The multi-layered implant includes a Metal Injection Molded body comprising a titanium alloy, a porous coating layer on a first surface of the Metal Injection Molded body, and a zirconium alloy layer on a second surface of the Metal Injection Molded body. The first surface and the second surface are on opposite sides of the Metal Injection Molded body. A zirconia layer may be formed over the zirconium alloy layer. The porous coating may be a titanium-based porous coating.

Abstract: The present invention is directed to a method and automated transfer means for transferring a container within an apparatus. The apparatus of the present invention may include a means for automated loading, a means for automated transfer and/or a means for automated unloading of a container (e.g., a specimen container). In one embodiment, the apparatus can be an automated detection apparatus for rapid non-invasive detection of a microbial agent in a test sample. The detection system also including a heated enclosure, a holding means or rack, and/or a detection unit for monitoring and/or interrogating the specimen container to detect whether the container is positive for the presence of a microbial agent. In other embodiment, the automated instrument may include one or more, bar code readers, scanners, cameras, and/or weighing stations to aid in scanning, reading, imaging and weighing of specimen containers within the system.

Abstract: A method and automated apparatus for rapid non-invasive detection of a microbial agent in a test sample is described herein. The apparatus may include one or more means for automated loading, automated transfer and/or automated unloading of a specimen container. The apparatus also includes a detection system for receiving a detection container, e.g., container or vial, containing a biological sample and culture media. The detection system may also include one or more heated sources, holding structures or racks, and/or a detection unit for monitoring and/or interrogating the specimen container to detect whether the container is positive for the presence of a microbial agent therein. In other embodiment, the automated instrument may include one or more, bar code readers, scanners, cameras, and/or weighing stations to aid in scanning, reading, imaging and weighing of specimen containers within the system.

Abstract: The present invention is directed to a method and automated loading mechanism for loading an apparatus. The apparatus of the present invention may include a means for automated loading, a means for automated transfer and/or a means for automated unloading of a container (e.g., a specimen container). In one embodiment, the apparatus can be an automated detection apparatus for rapid non-invasive detection of a microbial agent in a test sample. The detection system also including a heated enclosure, a holding means or rack, and/or a detection unit for monitoring and/or interrogating the specimen container to detect whether the container is positive for the presence of a microbial agent. In other embodiment, the automated instrument may include one or more, bar code readers, scanners, cameras, and/or weighing stations to aid in scanning, reading, imaging and weighing of specimen containers within the system.

Abstract: A method and automated apparatus for rapid non-invasive detection of a microbial agent in a test sample is described herein. The apparatus may include one or more means for automated loading, automated transfer and/or automated unloading of a specimen container. The apparatus also includes a detection system for receiving a detection container, e.g., container or vial, containing a biological sample and culture media. The detection system may also include one or more heated sources, holding structures or racks, and/or a detection unit for monitoring and/or interrogating the specimen container to detect whether the container is positive for the presence of a microbial agent therein. In other embodiment, the automated instrument may include one or more, bar code readers, scanners, cameras, and/or weighing stations to aid in scanning, reading, imaging and weighing of specimen containers within the system.

Abstract: An example method includes displaying a first control and a second control, wherein a touch associated with the controls results in moving an indicator through information in a first direction and in a second direction, in response to the detecting a first touch associated with the first control, moving the indicator in the first direction, and in response to detecting a second touch associated with the second control, moving the indicator in the first direction.

Abstract: The invention relates to a process for manufacturing a fixing device and a fixing device made by such a process. In particular, albeit not exclusively, the present invention relates a fixing device for application in fixing to concrete and like materials/substrates. The present invention therefore seeks to provide a fixing device for fixing to concrete, other like substrates which overcomes, or at least reduces some of the known problems of the prior art. The present invention also seeks to provide a fixing device which has enhanced corrosion resistance.

Abstract: The present invention is directed to a method and automated transfer means for transferring a container within an apparatus. The apparatus of the present invention may include a means for automated loading, a means for automated transfer and/or a means for automated unloading of a container (e.g., a specimen container). In one embodiment, the apparatus can be an automated detection apparatus for rapid non-invasive detection of a microbial agent in a test sample. The detection system also including a heated enclosure, a holding means or rack, and/or a detection unit for monitoring and/or interrogating the specimen container to detect whether the container is positive for the presence of a microbial agent. In other embodiment, the automated instrument may include one or more, bar code readers, scanners, cameras, and/or weighing stations to aid in scanning, reading, imaging and weighing of specimen containers within the system.

Abstract: The present invention is directed to a method and automated transfer means for transferring a container within an apparatus. The apparatus of the present invention may include a means for automated loading, a means for automated transfer and/or a means for automated unloading of a container (e.g., a specimen container). In one embodiment, the apparatus can be an automated detection apparatus for rapid non-invasive detection of a microbial agent in a test sample. The detection system also including a heated enclosure, a holding means or rack, and/or a detection unit for monitoring and/or interrogating the specimen container to detect whether the container is positive for the presence of a microbial agent. In other embodiment, the automated instrument may include one or more, bar code readers, scanners, cameras, and/or weighing stations to aid in scanning, reading, imaging and weighing of specimen containers within the system.

Abstract: An example method includes associating a first area of a non-display area of a touch-sensitive display with a first control, wherein a touch associated with the first control results in moving an indicator through the information in a first direction and in a second direction. The method may also include associating a second area of the non-display area with a second control, wherein a touch associated with the second control results in moving the indicator through the information in the first direction and in the second direction. The method may also include detecting a first touch associated with the first control, in response to detecting the first touch, moving the indicator in the first direction, detecting a second touch associated with the second control, and in response to detecting the second touch, moving the indicator in the first direction.

Abstract: A method, system and apparatus for imaging an oral cavity of a subject include a bracket comprising a mouthpiece and a camera mount. The mouthpiece has upper and lower bite guides disposed on a posterior side and separated by an opening through the mouthpiece. The bite guides are spaced apart so a subject biting on the guides opens the oral cavity to inspection through the opening. The mount is disposed on an anterior side of the mouthpiece; and has a flange to engage and slide along the opening and an optical path for light to pass through the mount and mouthpiece. A clip on an anterior side of the mount is configured to removeably hold a camera to record light passing through the optical path from the posterior side of the mount. In one embodiment, the camera is a programmable cell phone with digital camera.

Abstract: A transport system is provided for a sample testing machine. The transport system includes a carrier holding a set of test sample devices and a drive subsystem for moving the carrier through the sample testing machine. The drive subsystem includes a reciprocating motor-driven block engaging the carrier and moving the carrier back and forth in a predetermined longitudinal path extending along a longitudinal axis from an entrance station to a plurality of processing stations in the sample testing machine. The processing stations are accessed as the carrier is moved along the path. The carrier includes features in the form of slots or voids that are detected by strategically placed optical interrupt sensors. As the carrier moves, the slots are detected by the sensors to thereby continuously track the position of the carrier and the test devices as they are moved through the instrument.

Abstract: A method of stimulating neuronal growth or repair comprising exposing a target neuron or neuronal area to a solution of the metallothionein isoform MT-IIA.