Abstract: Systems and methods for quantifying a user capability in accordance with an organizational role are disclosed herein. In an aspect, a role capability assessment is deployed to a user comprising at least one question whereby the user selects at least one answer that corresponds to the at least one question and the at least one answer conveys information to determine the capability of the user to perform an organizational role. In another aspect, a set of answer data associated with the at least one answer is received whereby the set of answer data correlates to the capability of the user to perform a role within an organization.

Abstract: An implanted neural micro interface device is provided. The device comprises microfilaments of various materials and forms embedded within a body. The microfilaments form interaction sites with surrounding neural tissue at their exit points from the implantable body. The body and filaments are configurable in a multitude of positions to provide increased engagement of a given neural tissue section as well as interaction and closed loop feedback between the microfilament sites. Such configurations allow for a range of recording, stimulating, and treatment modalities for the device within research and clinical settings.

Abstract: Ingestible devices can directly deliver therapeutic agents to desired tissue(s) of the GI tract of a subject, such as the submucosa, the mucosa, and/or the mucus layer of the GI tract, and methods of using the same. The ingestible devices can deliver therapeutic agents in a safe, effective, and reliable manner. The disclosure also provides pharmaceutical compositions for use in methods of treating a disease or condition in a subject in need thereof.

Abstract: An apparatus for demonstrating the use of a medical device includes a body adapted for receiving the medical device. The body includes at least a portion adapted for viewing the medical device when positioned in the body. A cover is provided for selectively covering the portion of the body adapted for viewing the medical device. A kit and related methods are also disclosed.

Abstract: In some examples, a method of sensor degradation compensation is described. The method may include generating first characterization data for calibration of a first sensor, from amongst multiple sensors that include the first sensor and at least a second sensor, based on first sensor data generated by the first sensor. The method may further include providing the first characterization data to be pushed to the second sensor. The second sensor may be configured to be calibrated with the first characterization data. The method may also include collecting second sensor data generated by the first sensor and generating second characterization data based on the second sensor data after the first characterization data is provided. The method may further include providing the second characterization data to be pushed to the second sensor. The second sensor may be configured to be recalibrated with the second characterization data.

Abstract: In some examples, a device may include an orientation sensor, a device sensor, a sensor regime storage unit, an analysis module, and a device output module. The orientation sensor may generate orientation data indicative of a physical state of the device. The device sensor may generate device data. The sensor regime storage unit may store sensor regimes that process the generated device data while in the physical state. The analysis module may be coupled to the orientation sensor and the sensor regime storage unit, and may determine the physical state based on the generated orientation data and select a particular sensor regime based on the determined physical state. The device output module may be coupled to the analysis module and the device sensor, and may receive the particular sensor regime and process the device data using the particular sensor regime. The device may be implemented as a wearable sensor device.

Abstract: A method and apparatus for removing foreign matter, including debris and deposits and air bubbles from a flow cell of a particle study device. The apparatus includes a chamber with an aperture containing unit at one end and sample and sheath introduction mechanisms at the other end to supply respectively, a sample suspension of particles and a particle free liquid. The chamber has a waste orifice positionally disposed to provide a turbulent flow of particle free liquid within the chamber upon simultaneous injection and exhaustion of the particle free liquid into and out of, respectively, the sheath introduction mechanism and the waste orifice, to remove any air bubbles in the chamber and its adjacent aperture area.