Abstract: Systems and methods for providing automated inventory management of medicine and healthcare items stored within bins in care facilities are disclosed. A method includes providing an interactive storage device for attaching to a bin, and outputting, via an audiovisual element, a visual representation of a local inventory of the bin, receiving a user input, determining a change to the local inventory according to the user input, updating the local inventory in a non-volatile data store according to the change, synchronizing the local inventory with one or more nodes via a communication interface, and receiving, from the one or more nodes via the communication interface, periodic updates for a local cache comprising locations and inventories of one or more remote bins.

Abstract: An access control assembly is described herein. The assembly includes an actuator, a communication interface, a display, and a processor. The actuator is configured to open and close a latch to secure a door of the enclosure. The processor can be configured to receive a user credential for accessing the enclosure, validate the user credential for accessing the enclosure, trigger the actuator to open the latch, thereby allowing the door to be opened, and trigger the actuator to close the latch after detecting that the door is closed, thereby securing the door.

Abstract: Features relating to a wasting station that provides for secure collection, anonymous auditing, and safe disposal of medication are provided. The wasting station securely receives and stores wasted medication for later analysis. The wasting system may provide for waste containers that may include electronic tags, biomarkers, and/or reagents that may be used to analyze waste items. The wasting system may include support for witnessing the wasting process, either locally or remotely.

Abstract: A processing device receives operating data associated with one or more storage devices and analyzes the operating data using one or more artificial intelligence (AI) models to generate voltage threshold offsets for memory pages of the one or more storage devices. The processing device applies the generated voltage threshold offsets to read operations to read data from the memory pages. The AI models may be trained using data from other storage systems and can be executed by a storage system controller, by storage device controllers of the storage devices, or by both in a coordinated configuration. The disclosed techniques dynamically adjust voltage thresholds based on current device conditions to improve read accuracy, reduce error rates, and enhance overall system reliability and endurance.

Abstract: A method of detecting a fault condition in an infusion process, the method includes receiving a programmed flow rate pertaining to a fluid infusion provided by an infusion device; determining, a first weight of an infusion container associated with the fluid infusion provided by the infusion device at a first time; determining a second weight of the infusion container at a second time; determining based on the first weight and the second weight, a determined flow rate of the fluid infusion provided by the infusion device between the first time and the second time. The method includes determining a difference between the determined flow rate and the programmed flow rate. When a magnitude of the difference between the determined flow rate and the programmed flow rate satisfies a predetermined threshold, by the processor: causing an output of the infusion device or the weight sensor to indicate the fault condition.

Abstract: An integrated intravenous (IV) administration set includes a flow stop having a tubing fitment and a housing, the flow stop configured, in a first position, to prevent a flow of a fluid through the tubing, and in a second position, to permit the flow of the fluid through the tubing, the tubing fitment comprising a protrusion configured to receive a tubing. The IV administration set also includes an electronic flow sensor disposed within the housing, the electronic flow sensor configured to measure a flow of a fluid in the tubing, and one or more conductive connections configured within the housing and configured to provide electrical power to the electronic flow sensor. The flow stop is shaped to be loaded and engaged to a receptacle of an infusion device, and shaped to cause, when loaded and engaged, the one or more conductive connections to engage with a corresponding conductive connection provided by the infusion device to activate the flow sensor based on a power flow from the infusion device.

Abstract: Features relating to a wasting station that provides for secure collection, anonymous auditing, and safe disposal of medication are provided. The wasting station securely receives and stores wasted medication for later analysis. The wasting system may provide for waste containers that may include electronic tags, biomarkers, and/or reagents that may be used to analyze waste items. The wasting system may include support for witnessing the wasting process, either locally or remotely.

Abstract: Force sensing assemblies for an infusion pump are provided. A force sensing assembly includes a processor and an occlusion sensor coupled to the processor. The occlusion sensor is positioned opposed to an occluder valve when the platen is closed. The force sensing assembly measures one or more forces exerted on a fluid tube during a pump cycle. Infusion pump assemblies, methods of operating an infusion pump with a force sensing assembly, systems for controlling an infusion pump and an infusion device are also provided.

Abstract: Drip chamber detection assemblies for intravenous sets used with an infusion pump are provided. A drip chamber detection assembly includes a sensor coupled to a drip chamber. The sensor is positioned to generate signals related to the fluid level within the drip chamber. The signal data is transmitted to an infusion pump or a controller. A fluid level status or condition is determined and used for closed loop control of the infusion system, which generates an alarm and/or stops the infusion pump based on abnormal conditions. Methods of operating drip chamber detection assemblies are also provided.

Abstract: A locking cap assembly includes an upper housing; a lower housing rotatably connected to the upper housing and configured to be fitted onto a container; a near field communication (NFC) module configured to wirelessly receive a NFC input; an inductive charging coil; a microprocessor; and a latching mechanism, the latching mechanism includes a locking latch configured to prevent the upper housing and the lower housing from rotating with respect to each other; and an electrical actuation component configured to lock and unlock the latch and a current generated by the inductive charging coil. The lower housing includes a plurality of locking vanes within the lower housing, the locking vanes being configured to variably define an inner diameter size of the lower housing responsive to a rotation of the upper housing with respect to the lower housing when the lower housing is mechanically engaged with the container.

Abstract: Drip chamber detection assemblies for intravenous sets used with an infusion pump are provided. A drip chamber detection assembly includes a sensor coupled to a drip chamber. The sensor is positioned to generate signals related to the fluid level within the drip chamber. The signal data is transmitted to an infusion pump or a controller. A fluid level status or condition is determined and used for closed loop control of the infusion system, which generates an alarm and/or stops the infusion pump based on abnormal conditions. Methods of operating drip chamber detection assemblies are also provided.

Abstract: The present invention relates to heteroalicyclic compounds represented by the general formula (I), or their isotopic forms, stereoisomers, or pharmaceutically acceptable salts thereof. The present invention also describes a method of making such compounds, pharmaceutical compositions comprising such compounds and their use for the treatment or prevention of central nervous system related disorders.

Abstract: A locking cap assembly includes an upper housing; a lower housing rotatably connected to the upper housing and configured to be fitted onto a container; a near field communication (NFC) module configured to wirelessly receive a NFC input; an inductive charging coil; a microprocessor; and a latching mechanism, the latching mechanism includes a locking latch configured to prevent the upper housing and the lower housing from rotating with respect to each other; and an electrical actuation component configured to lock and unlock the latch and a current generated by the inductive charging coil. The lower housing includes a plurality of locking vanes within the lower housing, the locking vanes being configured to variably define an inner diameter size of the lower housing responsive to a rotation of the upper housing with respect to the lower housing when the lower housing is mechanically engaged with the container.

Abstract: Aspects of a storage device are provided for handling GBBs with defects between global interconnects and local word lines. The storage device includes a plurality of blocks each including a plurality of word lines, a plurality of interconnects within an interconnect set and between multiple ones of the blocks, volatile memory, and a controller. The controller determines a logical address pattern associated with the multiple ones of the blocks respectively including a program failure, determines whether the logical address pattern is associated with the interconnect set for the multiple ones of the blocks, determines a common word line associated with the program failures in the multiple ones of the blocks, un-marks these blocks as GBBs, and refrains from programming the common word line during respective program operations in the multiple ones of the blocks. Thus, blocks may be reclaimed, defective word line(s) isolated, and likelihood of read-only modes reduced.

Abstract: A method for remotely witnessing a medical workflow is provided. The method includes authenticating a clinician at a witnessing device. The method also includes receiving, at the witnessing device, a request to perform a medical workflow. The method further includes determining, at the witnessing device and based at least in part on the medical workflow, that a witness is required to observe the medical workflow. The method also includes initiating, at a witnessing client remotely coupled with the witnessing device, a witnessing session, wherein the witnessing client allows a witness to remotely observe the medical workflow. The method also includes enabling, in response to at least the initiation of the witnessing session, completion of the medical workflow. Related systems and articles of manufacture, including apparatuses and computer program products, are also disclosed.

Abstract: The present invention relates to substituted heterocyclic compounds represented by the general formula (I), or their isotopic forms, stereoisomers, or pharmaceutically acceptable salts thereof. The present invention also describes the method of making such compounds, pharmaceutical compositions comprising such compounds and their use in the treatment of central nervous system disorders.

Abstract: Disclosed herein are methods, systems and devices including a first layer with a first compute device, a first device stack, and a second device stack between the first device stack and the first compute device. A second layer may be mounted on top of the first layer. The second layer may include a first bridge electrically connecting the first compute device to the first device stack and a second bridge electrically connecting the first compute device to the second device stack.

Abstract: A mobile smart container system comprises a housing, an access component configured to secure access to a compartment within the housing when in a closed position, a communication interface configured to wirelessly receive a request to access the compartment, a perceivable output device, an electromechanical latch configured to engage with the access component to releasably lock the access component in the closed position, and a processor. The processor receives and authenticates the request to access the compartment and, in response to receiving and authenticating the request, activates the electromechanical latch to unlock the access component to make the compartment accessible, and outputs, upon actuation of the electromechanical latch, an alert via the perceivable output device to identify the smart container system.

Abstract: A method, system and devices are disclosed providing a first layer, the first layer including a first device region and a second device region, and a second layer including an interconnection die, the interconnection die including an interface logic. The first device region and the second device region are mounted on a first side of the interconnection die, and the first device region and the second device region are communicatively coupled to the interface logic.

Abstract: Disclosed herein are methods, systems and devices including a first layer, the first layer including a first compute device, a first multi-device package, and a second multi-device package. The first compute device may be between the first multi-device package and the second multi-device package. A second layer may include a first redistribution layer on a first side of the second layer facing the first layer, the first redistribution layer electrically connecting the first compute device to the first multi-device package and the first redistribution layer electrically connecting the first compute device to the second multi-device package. The first layer may include a third multi-device package and a fourth multi-device package, with the first compute device between the third multi-device package and the fourth multi-device package.