A system for operating an inhalation device including an inhalation device that has been configured to store at least one substance and dispense the substance in a predetermined manner, wherein the inhalation device is configured to gather usage information from the inhalation device and transmit the gathered usage information to a location remote from the inhalation device and to receive operational commands from a location remote from the inhalation device; a controller in communication with the inhalation device, wherein the controller is configured to receive usage information from the inhalation device and to transmit operational commands to the inhalation device; and a remote server in communication with the controller, wherein the remote server is configured to receive queries from the controller, and transmit information relevant to the queries back to the controller.

A nebulizer as well as a container with a fluid for such a nebulizer are proposed. The container comprises a control device which indicates initially an unused state of the container before first use. An indicator device stops via a locking device further use of the container in a locked state when a predetermined number of uses has been reached or exceeded. After replacement of the container, the nebulizer can be reset and used again.

A breath actuated metered dose inhaler may comprise a canister fire system configured to fire a medicament containing canister in response to patient inhalation. The canister fire system may comprise a pneumatic force holding unit and having a rest configuration in which a metering valve of the canister is in a refill configuration; a prepared configuration in which a canister actuation force is retained by the pneumatic force holding unit and the canister fire system is actuatable by patient inhalation induced airflow; and a fire configuration in which the metering valve is in a dose delivery position. When in the prepared configuration, the force retained by the pneumatic force holding unit may be reduced by less than about 6% over a period of 5 minutes, preferably less than about 3% over a period of 5 minutes.

The invention relates to a spray device having a spray nozzle unit and at least one further spray nozzle unit. Each spray nozzle unit has at least one spray nozzle body, wherein said at least one spray nozzle body comprises a chamber for receiving a pressurized fluid. Said chamber is bounded by a spray wall having at least one spray orifice that extends through said spray wall and opens to an external environment. Each of said at least one orifice in a spray wall has a substantially identical predetermined size lying in a predetermined range and releases a mono disperse spray jet of the pressurized fluid fed from the associated reservoir. Said range within said first spray nozzle unit differs from said range within said at least one further spray nozzle unit, particularly said ranges do not overlap.

A device is designed to put the inhaler into a triggering-ready state by adding energy to a stored energy source of the inhaler. The inhaler can be inserted into the device and/or mechanically coupled to the device in order to put the inhaler into the triggering-ready state.

A drive mechanism for a medicinal inhaler, the inhaler comprising: a patient port; a canister actuable by the drive mechanism to deliver a dose of medicament to the patient port, the drive mechanism comprising: a follower which moves between a first position in which the mechanism is primed for use and a second position in which the follower engages the canister to deliver a dose of medicament to the patient port, the follower being carried on a rocker plate which pivots as the follower moves between its first and second position, wherein the rocker plate engages a switch when the follower is in its second position to indicate that a dose of medicament has been delivered to the patient port.

Systems and methods for integrating a continuous glucose sensor 12, including a receiver 14, a medicament delivery device 16, a controller module, and optionally a single point glucose monitor 18 are provided. Integration may be manual, semi-automated and/or fully automated.

A nasal applicator for nasally applying medicinal active ingredients, comprising a dispensing pin which is introduced into a nostril, a active ingredient store arranged in an applicator housing, and a dispensing metering device. A transmitting device is designed to be engageable and disengageable between an actuation button and the dispensing metering device such that when the transmitting device is disengaged, the actuation button is moved in the open passage without a transmission to the dispensing metering device. A movement sensor is provided for detecting movements of the operating button, and a coupling switch is provided for engaging the transmitting device depending on a signal of the movement sensor. To generate a consistent spray pattern, the dispensing metering device comprises a pretensioning mechanism which is tensioned or released to actuate a metering conveyor with a defined pretensioning force, wherein the engaged transmitting device can tension or release the pretensioning mechanism.

Systems and methods for isolating and/or desiccating a portion of a drug delivery tract of a drug delivery apparatus to reduce water vapor content therein are provided. For example, there is provided a metered dose inhaler for delivering aerosolized medicament or other matter to a user. The aerosolized medicament or other matter may be discharged from a discharge passageway within the inhaler into an inhalation passageway for inhalation by a user, and the inhaler may comprise a seal member operative to selectively isolate the discharge passageway from the inhalation passageway and external environment during inactivity. The inhaler may further comprise a desiccant material arranged to withdraw moisture from the isolated discharge passageway. In other instances, desiccant material may be arranged to withdraw moisture from the discharge passageway of the inhaler without isolating the discharge passage during inactivity.

Some embodiments are directed to a compliance monitor for monitoring patient usage of a medicament inhaler, the medicament inhaler including a store of medicament, a first housing for housing the store of medicament, a medicament dispenser for delivering a dose of medicament, a mouthpiece for directing the dose of medicament into the mouth of the patient, and a removable and replaceable cap for the mouthpiece. The compliance monitor includes a cap detector, such as a switch, for determining when the cap is covering the mouthpiece and/or for determining that the cap is being removed or replaced, with respect to the mouthpiece. The compliance monitor may also include a dose detector, such as a switch, for determining that a dose of medicament has been dispensed. Furthermore the cap is attached to the first housing by a tether or hinge.