摘要:
The present invention is a method featuring containers for consumable products which have removable sample compartments to facilitate reuse, product returns post-trial, and product resale. The sample compartments are filled with the same product as the main compartment so that consumers may sample the product without damaging a tamper-proof seal on the main compartment. The used sample container may be refilled or replaced with a new sample container. Use of these containers may reduce waste by preserving the product in the main container in a sealed condition. Use of these containers may also minimize the return expense of products sold online by giving the consumer a chance to try the product and return the main container if they are unsatisfied, ultimately reducing the overall the cost per product and reducing the waste of both product and container or container materials.
摘要:
An insulated packaging assembly can include a box including a top side wall, a bottom side wall, a first lateral side wall, a second lateral side wall, a third lateral side wall, and a fourth lateral side wall, the box defining a cavity; a first thermal liner positioned in the cavity, a first portion of the first thermal liner positioned in contact with the top side wall, a second portion of the first thermal liner positioned in contact with the first lateral side wall, a third portion of the first thermal liner positioned in contact with the bottom side wall; and a second thermal liner positioned in the cavity, a first portion of the second thermal liner positioned in contact with the second lateral side wall, a second portion of the second thermal liner positioned in contact with the third lateral side wall.
摘要:
To provide a drug discharge device capable of reducing complexity when distributing a drug into a manual distribution device. A drug discharge device includes a manual distribution member 15 that includes a plurality of recessed portions 20 in which a solid drug is distributed, discharge means that discharges the drug distributed in the recessed portions 20 to a downstream side directly or via another member, and a control device that controls the discharge means, in which the discharge means is capable of individually discharging a drug corresponding to a predetermined recessed portion 20, the control device assigns the same drug to the recessed portions 20 in adjacent regions based on prescription information including information on a drug to be provided to a plurality of patients or one patient, and the discharge means discharges the drugs in a predetermined order.
摘要:
A nested insulated packaging assembly comprising an outer box and a thermal liner. The outer box includes an outer top side wall, an outer bottom side wall, and a plurality of outer lateral side walls. The thermal liner includes a terminal top end, a bend line, a top fold defined between the terminal top end and the bend line, and a back fold. The top fold is foldable relative to the back fold at the bend line. The back fold contacts one of the outer lateral side walls of the outer box. The thermal liner includes a thermal control material extending across the bend line.
摘要:
A manufacturing method of two-chamber type combined container-syringe including: a vacuum plugging process (S2) of eliminating air bubbles from the dissolving solution of the dissolving solution-filled cartridge and sealing the dissolving solution with a middle stopper after the dissolving solution filling process (S1); a vacuum plugging process (S2) has a first cooling processing (S21) of cooling the inside of a vacuum plugging equipment in which a dissolving solution-filled cartridge is disposed to a cooling temperature that does not freeze the dissolving solution, a first decompression processing (S23) of decreasing a pressure inside the vacuum plugging equipment while the vacuum plugging equipment maintains the cooling temperature after the first cooling processing (S21), and a middle stopper pushing processing (S24) of pushing the middle stopper downward and bringing the middle stopper into contact with the dissolving solution after the first decompression processing (S23). The dissolving solution can be easily filled in a bubble-free state in the two-chamber type combined container-syringe.
摘要:
A flexible pouch and a method for making a flexible pouch is provided. The pouch includes a pouch body defined by a peripheral edge. A dividing seal is disposed between opposite ends of the flexible pouch so as to define two pouch spaces. The pouch includes two fitments are mounted to a respective pouch space. One of the fitments is configured to support the pouch body in an upright manner. A method for making said flexible includes forming a flexible pouch having an open top. A dividing seal extends from the open top to the bottom of the pouch so as to define two pouch openings and two pouch spaces. Substances are introduced into the pouch spaces by a first nozzle and a second nozzle inserted into a respective first space and second space and filling the pouch body through the first and second nozzle.
摘要:
A method of filling a cartridge having one or more pouches. The method may include the steps of placing the pouch on a support, placing a first cartridge half over the pouch and the support, placing the pouch and the first cartridge half on a second cartridge half to form the cartridge, maneuvering the cartridge to a filling unit, and filling the pouch within the cartridge.
摘要:
A package includes a first pouch and either a second pouch or a cover, where the pouches are configured to contain a product, such as a food product, and attached relative to each other about a hinge. The package includes at least one closure flap. The first and second pouches or first pouch and cover are movable about the hinge from a closed position where access is at least partially blocked by the closure flap toward an open position where the closure flap is separated to allow greater access. Methods of manufacturing such packages are also provided.
摘要:
A device for accommodating a freeze-dried pharmaceutical product (S) for reconstitution, comprising: a vessel (1) having at its opening end (3) an opening edge (4) and an adjoining longitudinal portion (5) with an evenly formed inner cross section, a front plunger (2) to be positioned inside the vessel (1) at the longitudinal portion (5), wherein the front plunger (2) is configured to be positioned inside the vessel (1) in a sealing state, in which the front plunger (2) is fully inserted in the vessel (1), or in an exchange state, in which the front plunger (2) is inserted partly in the vessel (1) and partly protrudes over the opening edge (4) of the vessel (1), and wherein the front plunger (2) comprises sealing means that are configured to seal the inside of the vessel (1) against the outside when the front plunger (2) is positioned in the sealing state, and one or more communicating grooves (2i) that are configured to place the inside and outside of the vessel (1) in communication with each other when the front plunger (2) is positioned in the exchange state, is characterized in that the sealing means are dimensioned and/or structured in such a way that the front plunger (2), when an underpressure of predefined strength is applied to the outer environment of the vessel (1), is caused to move inside the vessel (1) toward its opening end (3). Furthermore, a method of manufacturing a sealed vessel (1) accommodating a freeze-dried pharmaceutical product (S) is disclosed.
摘要:
Soluble pouches are formed on a continous motion rotating thermoforming machine having cavities in the surface of a drum into which a web of polymeric film is drawn by a vacuum to form pockets. The pockets are filled with one or more components and closed by a further web of polymeric film. Shrink-back of the polymeric film within the cavities is reduced by heating the cavities with heaters.