An inhalation device for delivering medication to a user may include a mouthpiece, a dosing chamber, and a flow channel connecting the mouthpiece to the dosing chamber. The dosing chamber may be configured to deliver the medication to the user via the mouthpiece. The inhalation device may include an electronically driven vibratory element, a sensor system configured to generate a pressure signal indicative of air flow through the flow channel, and a controller. The controller may be configured to receive the pressure signal from the sensor system (e.g., a micro-electrical mechanical (MEMS) pressure sensor). The controller may be configured to perform an inhalation detection procedure to determine a plurality of successful inhalations. For example, the controller may be configured to generate a trigger signal to control timing of operation of the electronically driven vibratory element to release medication into the dosing chamber based on the plurality of successful inhalations.

Small-volume oral transmucosal dosage forms or NanoTabs comprising a predetermined amount of a pharmaceutically active drug are provided. Exemplary applications include use of the NanoTabs to administer a drug for the treatment of acute, post-operative or breakthrough pain.

A vaporizing article, comprises a vaporizer drive circuit; one or more memories configured to store a percentage of at least one constituent in an inhalation media, one or more compensation values for at least one compensation category for the at least one constituent, and instructions; and a control circuit comprising a processor coupled with the one or more memories configured to run the instructions, the instructions configured to cause the processor to: receive a dose target for a constituent; determine whether to perform compensation for an inhalation media dose in order to ensure the dose target is met; when compensation is to be performed, determine the properly compensated inhalation media dose based on an associated compensation value for the constituent; and control the vaporizer drive circuit so as to dispense a compensated dose of the inhalation media.

An inhaler includes a mouthpiece cover, a pressure sensor, a first indicator and a second indicator. The first indicator may be configured to indicate based on a state of the cover, and the second indicator may be configured to indicate based on an output of the pressure sensor. For example, when the mouthpiece cover opens, the first indicator may illuminate and a dose of medication may be transferred from a reservoir to a dosing cup. The second indicator may illuminate if an amount of inhaled medication reaches a predetermined threshold for successful inhalation.

The present disclosure relates to a heating inhaler and a controlling method thereof. The method includes: the sensing element detecting a suction action, and if the sensing element detects the suction action within a first predetermined time period, the control circuit board controlling the power source to supply power to the atomizer for a second predetermined time period then stop supplying, wherein the indicating element displays a first state within the second predetermined time period until the power source stops supplying power to the atomizer, then the indicating element displays a second state. If the sensing element detects no suction action within the first predetermined time period, the control circuit board controlling the power source to stop supplying the electric power to the atomizer, and the indicating element displaying the second state.

A smoke inhalation apparatus may include a cartridge including a release device configured to release a substance, a controller configured to control the operation of the release device, and a communication device configured to allow a user to change and monitor settings of the smoke inhalation apparatus and/or a state of the smoke inhalation apparatus. The communication device may include a sensor configured to be activated by tapping a predetermined number of times at a minimum frequency.

Security features for an electronic metered-dose smart inhaler, mobile app, and cloud-based software system for use with medical prescriptions and clinical trial regimens. The smart inhaler requires several types of user validation and feedback, and enters a locked-out state when required user feedback is not received or when received user feedback raises a suspicion of fraudulent or improper use. While the smart inhaler system is well suited for aerosol medical marijuana products, it may be used to deliver and conduct clinical trials on any type of product suitable for aerosol administration including other types of medication and non-medical products, such as nicotine, herbal products, pain killers, sleep aids, dietary stimulants, dietary suppressants, etc. The security features are not limited to aerosol inhalers, and may be applied more widely to other types of in-home, patient-administered products.

Provided is a fine particle generating apparatus outputting usage information, and in particular, a fine particle generating apparatus that generates fine particles through electrical heating and outputs usage information thereof to a user. Also, provided is a fine particle generating apparatus that generates fine particles by determining whether a puff has occurred according to a temperature variation amount per unit time. Also, provided is a fine particle generating apparatus or an aerosol generating apparatus capable of changing puff conditions by controlling a heater. Also, provided is a fine particle generating apparatus that generates fine particles through electrical heating.

A respiratory system and method comprise a tracker module adaptable to be secured to a variety of inhalers, the tracker module sensing activation of the medication canister of the inhaler for delivery of medication to a user. The tracker module also senses the rate of inhalation air flow of the user when inhaling medication for determination of proper inhaler use. Upstream and downstream sensors provide flow information to determine quality of the inhalation. A flow sensor is an integral part of the tracking module and can be used on multiple inhalers. Other sensors are provided that monitor user presence at the inhaler, user technique in using the inhaler, and the attitude of the inhaler when it was used. Low power devices are used to conserve battery power. A spirometer provides user lung function data.

A monitoring connector for a patient ventilation system serves for connecting to a breathing air tube portion for conducting ventilation air to a patient and for connecting the breathing air tube portion to a patient air interface. The connector has a control/regulation unit and at least one sensor for capturing a breathing air parameter which is in signal communication with the control/regulation unit. According to one aspect, the connector has a signal data memory for at least temporarily storing signal data. According to a further aspect, the sensor is configured as to measure the breathing air parameter in contact with the breathing air. According to one further aspect, the sensor is configured as to measure the breathing air parameter without contact. According to another aspect, the control/regulation unit has a plurality of signal transmission interfaces. This results in a connector which can be used flexibly and adapted to the respective requirements.