A simple and quick verification of the authenticity of a blister of elements, such as pills in the pharmaceutical industry, is provided. The pills packaged in a blister can be authenticated using mobile imaging devices such as a mobile smartphone. Generally speaking, an image of the pills and their differentiating physical characteristics in the blister is acquired and compared to at least one code which is marked on the blister itself. This code may also be encrypted. A dedicated software application on the mobile smartphone can be used to decrypt the code and compare the code to the image of the pills in the blister, to thereby evaluate authenticity of the blister and its contents.

A tray (100) for accommodating a coiled medical device, such as a catheter assembly (700), includes a first compartment (101), a second compartment (102), and a third compartment (103). The catheter assembly (700) and devices associated with a catheterization procedure, such as syringes (701,702) containing sterile water and lubricating jelly and a specimen container (703) can be disposed within the tray. Printed instructions (1001) can be included with the tray (100). One or more layers of wrap material (2200) can be folded about the tray (100) to enclose the tray (100) and other items, such as an additional layer of wrap material (2701), packaged liquid hand sanitizer (2401), and packaged gloves (2402). When a health care services provider (3101) unfolds the wrap material, the same can be used to create a sterile field beneath a patient (3201).

A tracking and tracing method is provided during the life of the pharmaceutical container to improve the safety and efficacy of the pharmaceutical container and its content. An identification code is added to the surface of the pharmaceutical container, which is not visible under ambient light. The identification code contains encrypted information regarding temporal and physical properties of the pharmaceutical container and pharmaceutical fluid content. At multiple stages during the life of the pharmaceutical container the identification code is detected with an optical detection method. Given the material of the identification code, the identification code is only visible by using specific optical detection methods.

Introduced here are containers designed to promote compliance with regimens for administering the medications stored therein. These containers can facilitate the conveyance of information related to a regimen through the use of a non-written medium. A container may include one or more display elements configured to emit/reflect light to indicate when medication stored in the container should be administered. An example of a display element is a light-emitting diode (LED). Emittance/reflectance of the light by the display element(s) may be governed by a different clock signal than the clock signal used to determine whether doses of medication are due to be administered.

A time programmable container for timing an object, includes a base for containing the object, a lid for sealing the base, and a spacer which is positioned intermediate the lid and the base. The spacer is positionable in a select one of a plurality of positions on the base. The spacer and the base contain time indicia such that each of the plurality of positions that the spacer can be placed upon the base corresponds to a different of time indication. The base includes a device to secure the spacer in the select one position to inhibit the movement or rotation of the spacer with respect to the base. The securing device includes a finger on the base that cooperates with or mates with a corresponding depression of the spacer. The cap removal inhibiting device includes a cavity on the bottom surface of a lip of the lid, with the lip circumventing the cap, and further includes a tab on the upper surface of the spacer with the tab positioned on the spacer and configured to mate with the cavity of the lid, such that when the spacer is placed upon the base and the lid is threaded onto the base, the tab of the spacer extends into the cavity of the lid, thereby securing the spacer onto the base and further preventing the removal of the lid from the base without first removing the tab from the cavity.

A tray (100) for accommodating a coiled medical device, such as a catheter assembly (700), includes a first compartment (101), a second compartment (102), and a third compartment (103). The catheter assembly (700) and devices associated with a catheterization procedure, such as syringes (701,702) containing sterile water and lubricating jelly and a specimen container (703) can be disposed within the tray. Printed instructions (1001) can be included with the tray (100). One or more layers of wrap material (2200) can be folded about the tray (100) to enclose the tray (100) and other items, such as an additional layer of wrap material (2701), packaged liquid hand sanitizer (2401), and packaged gloves (2402). When a health care services provider (3101) unfolds the wrap material, the same can be used to create a sterile field beneath a patient (3201).

A reminder system and methods may be configured for medicine regimen compliance and monitoring. Embodiments may include a control device, a medicine container, a medicine identifier attachable to the medicine container, a medicine container input device, a monitoring device having an adaptor to receive a medicine container, and a portable electrical device. The adaptor may be configured to releaseably couple the monitoring device and the medicine container. The control device, the medicine container input device and the monitoring device may include microprocessors, memories, input devices and output devices. The control device may provide operations including input and compare a prescription and medicine information. The monitoring device may provide operations including compare the medicine identifier of the medicine container and the medicine information. The monitoring device may also provide operations including determining the amount of medication removed from the medicine container. The operations may further include generate, by the output device, an alert in response to the distance exceeding a threshold.

This drug-supplying device is provided with: a rotator that discharges drugs towards the outer diameter by being rotated; a drug shape-specifying unit for specifying the shape of the drug; and a control unit that rotates the rotator at a rotational speed specified, on the basis of a speed table that correlates drug shape to rotator rotational speed, by the shape that has been specified by a drug-detecting unit.

A drug dispenser assembly comprising: a drug dispenser for dispensing a drug in a dispense event; and a skinprint analyser configured to receive a skinprint, preferably a fingerprint, of a user. The skinprint analyser is further configured: to perform a verification test regarding the identity of the skinprint; to conduct a chemical analysis for the presence of a metabolite in the skin-print; and to produce data indicative of results of the verification test and the chemical analysis. The drug dispenser assembly further comprises an actuator configured to actuate a dispense event in the event that the results of one or both of the verification test and the chemical analysis meet one or more predetermined conditions.