A pharmaceutical packaging system includes a substrate having a first surface, a first hollow cavity accessible through a first opening in the first surface, and a second hollow cavity accessible through a second opening in the first surface. The first and second hollow cavities are spaced apart and isolated from one another on the substrate. A cover is attached to at least a first portion of the first surface of the substrate surrounding the first opening and a second portion of the first surface of the substrate surrounding the second opening so as to provide a first seal for the first hollow cavity and a second seal for the second hollow cavity. At least one orally-administered medicament is contained within one of the first and second hollow cavities, and a first topically-applied medicament is contained within the other of the first and second hollow cavities.

An apparatus for medication management. The apparatus includes a housing for a packet of medication, a sensor coupled to the housing for sensing whether the packet has been removed or is likely to have been removed from the housing, and a transmitter for wirelessly transmitting data regarding a reading of the sensor to a remote computer. A system for medication management communicates with the apparatus for medication management is provided. The remote computer is configured to send an alert to an external device, and the alert is based on the reading of the sensor. Also, an apparatus for medication management includes a housing for medication, and a sensor for sensing a quantity of medication within the housing. The sensor includes a plurality of conductive electrodes arranged in an interleaved pattern, and provided in a substantially horizontal position. Related systems, methods, techniques and articles are also disclosed.

Described herein is dispensing cup for use with medicaments, which dispensing cup in use allows for the patient to (self) administer an oral medicament (tablet or capsule) without the need to come into direct (skin) contact with such medicament.

A container for a packaging assembly can include a body having a base and a sidewall extending therefrom. The body can define an interior including a product space configured for housing at least one product, and can have an opening leading to the interior. The container can include an active agent located within a compartment that is provided within the interior. The compartment can be sealed by a sealing layer to encapsulate the active agent within the compartment so as to prevent fluid communication between the active agent and the product space.

In one example, the present disclosure describes a device, computer-readable medium, and method for monitoring a patient's medication adherence. In one example, an apparatus includes a set of contact pins to electrically engage a conductive trace circuit of a unit dose packaging and to generate a signal in response to a break in the conductive trace circuit, a processor comprising a plurality of analog channels to detect and record the signal, a cellular modem to send, via a data network to which the apparatus is connected, information about the signal to a medication adherence monitoring service, a housing containing the set of contact pins, the processor, and the cellular modem, wherein the housing is configured for removable insertion of the unit dose packaging, and a lock to reversibly lock the unit dose packaging in the housing.

Introduced here are containers designed to promote compliance with regimens for administering the medications stored therein. These containers have various features that allow them to be more easily managed by the individuals to whom the medications were prescribed. Some features improve the ease with which containers communicate with individuals. These features may enable information to be more easily input by individuals and/or output for individuals in a comprehensible manner. Other features improve the mechanical or electrical durability of containers. Such features may enable the containers to be used by individuals over the course of several days, weeks, or months without worrying about structural damage or loss of power.

In various aspects, the present disclosure pertains to thermoformed webs that comprise polymer films having one or more thermoformed cavities contained therein, the polymer films comprising a polymer blend of amorphous polyethylene terephthalate (APET) and a copolyester that comprises (a) dicarboxylic acid residues (e.g., dicarboxylic acid residues that comprise terephthalic acid residues and, optionally, one or more additional dicarboxylic acid residues) and (b) diol residues (e.g., diol residues comprising ethylene glycol residues and, optionally, one or more additional diol monomer residues). Other aspects of the disclosure pertain to methods of forming such thermoformed webs, packaged products comprising such thermoformed webs, and methods of recycling such thermoformed webs.

In various aspects, the present disclosure pertains to thermoformed webs that comprise polymer films having one or more thermoformed cavities contained therein, the polymer films comprising a polymer blend of amorphous polyethylene terephthalate (APET), polyethylene furanoate (PEF), and a copolyester that comprises (a) dicarboxylic acid residues (e.g., dicarboxylic acid residues that comprise terephthalic acid residues and, optionally, one or more additional dicarboxylic acid residues) and (b) diol residues (e.g., diol residues comprising ethylene glycol residues and, optionally, one or more additional diol monomer residues). Other aspects of the disclosure pertain to methods of forming such thermoformed webs, packaged products comprising such thermoformed webs, and methods of recycling such thermoformed webs.

Package for components of aerosol generating devices, comprising: at least two components; a sleeve comprising a first wall and a second wall opposite and parallel to each other, and a first opening and a second opening opposite to each other; a first and a second blister pack containing the components and slidable relative to the sleeve through the first opening and the second opening, respectively; a first guide flap extending from the second wall of the sleeve at the second opening to create a first slot with the second wall; a second guide flap extending from the first wall of the sleeve at the first opening to create a second slot with the first wall; a first sliding flap integral with the first blister pack and a second sliding flap integral with the second blister pack which are arranged in the first slot and in the second slot, respectively, and that are shaped to slide in the first slot and in the second slot, respectively.

A medicine removal detection system is provided that includes a medication device and a storage member in a sheet shape storing the medication device. The medication device includes medicine, a secondary battery, and a signal transmission unit that transmits a signal indicating a state of the secondary battery. The storage member includes the electric current supply line for supplying an electric current to the secondary battery of the medication device, and is configured such that a supply environment of an electric current to the secondary battery changes when the medication device is taken out. The signal transmission unit transmits a signal indicating a state change of the secondary battery based on a change in the supply environment of an electric current to the secondary battery of the storage member.