The field of the present disclosure relates generally to packaging containers for shipping a product and, more particularly, to a container assembly for storing and transporting one or more units of temperature-sensitive products.
Containers are frequently utilized to store and aid in transporting products. These containers can be square, hexagonal, or octagonal, for example. At least some known products stored or transported in the containers require temperature-controlled environments to prevent spoliation of the products during transportation and delivery of the products to a consumer. In particular, at least some pharmaceutical products may be required to be maintained in a temperature-controlled environment even during shipment of the products to a consumer. In at least some cases, such pharmaceutical products that require a temperature-controlled environment are shipped in several large, multi-layered containers. These known containers are generally bulky and heavy, which increases shipping costs and makes it difficult for patients to carry and gain access to the pharmaceutical products.
In one aspect, a blank assembly is provided. The assembly includes a first blank for forming a carrier portion. The first blank includes a plurality of side panels for forming side walls of the carrier portion, the plurality of side panels including at least a first, second, third, and fourth side panel, and a joining tab, wherein the plurality of side panels at least partially define a cavity of the carrier portion. The assembly also includes a second blank for forming an internal divider insert. The second blank includes two opposing side edges, a plurality of fold lines that define a plurality of minor divider panels, and a cut line defined in at least one of the minor divider panels to define a securing tab positioned between the two side edges. The plurality of minor divider panels are configured to fold about the plurality of fold lines such that the securing tab moves outward from the cut line. When formed, the internal divider insert is positionable within the cavity of the carrier portion such that a carton insertion slot is at least partially defined by the securing tab and at least one side wall of the carrier portion.
In another aspect, a container assembly formed from a plurality of blanks of sheet material is provided. The assembly includes a carrier portion including a plurality of side walls and a bottom wall, wherein the plurality of side walls and the bottom wall at least partially define a cavity of the carrier portion. The assembly also includes an internal divider insert including two opposing side edges, a plurality of fold lines that define a plurality of minor divider panels, and a cut line defined in at least one of the minor divider panels to define a securing tab positioned between the two side edges. The plurality of minor divider panels are folded along the plurality of fold lines such that the securing tab moves outward from the cut line, and wherein the internal divider insert is positionable within the cavity of the carrier portion such that a carton insertion slot is at least partially defined by the securing tab and at least one side wall of the carrier portion.
In another aspect, a container assembly formed from a plurality of blanks of sheet material is provided. The container assembly includes a carrier portion including a plurality of side walls and a bottom wall, wherein the plurality of side walls and the bottom wall at least partially define a cavity of the carrier portion. The assembly also includes a shipping container portion including a plurality of side walls and a bottom wall, wherein the plurality of side walls and the bottom wall at least partially define a cavity of the shipping container portion. The shipping container portion also includes a plurality of thermal insulation panels positioned within the cavity of the shipping container portion, the plurality of thermal insulation panels defining a thermally insulating cavity sized to receive the carrier portion.
In yet another aspect, a method of forming a container assembly from a plurality of blanks of sheet material is provided. The method includes forming a carrier portion that includes a plurality of side panels for forming side walls of the carrier portion. The plurality of side panels include at least a first, second, third, and fourth side panel, and a joining tab, wherein the plurality of side panels at least partially define a cavity of the carrier portion. The method also includes forming an internal divider insert that includes two opposing side edges, a plurality of fold lines that define a plurality of minor divider panels, and a cut line defined in at least one of the minor divider panels to define a securing tab positioned between the two side edges. The plurality of minor divider panels are folded along the plurality of fold lines such that the securing tab moves outward from the cut line. The method also includes positioning the internal divider insert within the cavity of the carrier portion such that a carton insertion slot is at least partially defined by the securing tab and at least one side wall of the carrier portion.
The following detailed description illustrates the disclosure by way of example and not by way of limitation. The description enables one skilled in the art to make and use the disclosure, describes several embodiments, adaptations, variations, alternatives, and use of the disclosure, including what is presently believed to be the best mode of carrying out the disclosure.
A container assembly and blanks for constructing the same are described herein. More specifically, a container assembly, that may include an internal divider insert, and methods for forming the same are described herein. As described herein, the container assembly may include multiple embodiments. The resulting container is portable, provides shipping stability for products transported therein, and provides an efficient way to transport temperature-sensitive products. In addition, as described in greater detail below, the resulting container, which may be used to transport pharmaceutical products, also provides an adherence tracking system that enables a patient to track and manage the dates and times of taking the pharmaceutical products shipped in the container. It will also be apparent to those skilled in the art and guided by the teachings herein provided that the invention is likewise applicable to any storage container including, without limitation, a carton, a tray, a box, or a bin.
In one embodiment, the container assembly may be fabricated using at least one of a corrugated board and paperboard material. The container assembly, however, may be fabricated using any suitable material, and therefore is not limited to a specific type of material. In alternative embodiments, the container assembly is fabricated using cardboard, plastic, and/or any suitable material known to those skilled in the art and guided by the teachings herein provided.
Embodiments of the present disclosure provide a container assembly that facilitates storing and/or transporting temperature-sensitive products, such as pharmaceutical products, such as a tumor necrosis factor (TNF) inhibiting anti-inflammatory drugs (e.g., adadalimumab). More specifically, the container assembly includes a thermally insulated shipping container portion, a carrier portion sized for insertion within the shipping container portion, and, in some embodiments, an internal divider insert positionable within the carrier portion. The internal divider insert facilitates partitioning an internal cavity of the carrier portion into multiple carton insertion slots. Each carton insertion slot is sized to receive a single carton, which contains one or more doses of a pharmaceutical product, for example. As such, partitioning the internal cavity of the carrier portion with the internal divider insert enables a supplier to select the number of units to deliver to a patient in a single shipment while ensuring the units are secure within the carrier portion even though it may not be at full capacity. Moreover, once delivered, the carrier portion is easily portable and capable of being transferred directly from the shipping container portion to a refrigeration unit without having to remove the individual units from the carrier portion. In one embodiment, one or more side walls of the carrier portion may provide a location for an adherence tracking system, which may be configured to allow a patient to monitor and/or track a drug regimen (i.e., a time, a date, and/or a dosage amount taken). As described below, the adherence tracking system may be configured to communicate with a server system via a remote computing device, wherein the remote computing device includes a patient application stored thereon for enabling transmission of patient adherence data to the server system for storage and/or processing.
In another embodiment, the container assembly includes the thermally insulated shipping container portion and the carrier portion sized for insertion with the shipping container portion. However, in this embodiment, the container assembly does not include the internal divider insert. Rather, the carrier portion is sized to receive a single container of the pharmaceutical product. Thus, in this embodiment, the carrier portion is smaller than the other embodiment where the carrier portion is sized to receive the internal divider insert and up to three cartons of the product. Of course, the carrier portion could be sized to receive one or more cartons without the internal divider insert received therein.
In one embodiment, the container assembly and/or blanks may include at least one marking thereon including, without limitation, indicia that communicates the product, a manufacturer of the product, and/or a seller of the product. For example, the marking may include printed text that indicates a product's name and briefly describes the product, logos and/or trademarks that indicate a manufacturer and/or seller of the product, and/or designs and/or ornamentation that attract attention. In another embodiment, the container assembly is void of markings, such as, without limitation, indicia that communicates the product, a manufacturer of the product, and/or a seller of the product. Furthermore, the container assembly may have any suitable size, shape, and/or configuration (i.e., number of sides), whether such sizes, shapes, and/or configurations are described and/or illustrated herein. For example, in one embodiment, the container assembly includes a shape that provides functionality, such as a shape that facilitates transporting the container and/or a shape that facilitates stacking and/or arranging a plurality of containers.
Referring now to the drawings,
First major side panel 22 extends from joining tab 20 along fold line 30, first minor side panel 24 extends from first major side panel 22 along fold line 32, second major side panel 26 extends from first minor side panel 24 along fold lines 34, and second minor side panel 28 extends from second major side panel 26 along fold line 36. Fold lines 30, 32, 34, and 36 as well as other fold lines and/or hinge lines described herein, may include any suitable line of weakness and/or line of separation known to those skilled in the art and guided by the teachings herein provided.
First blank 10 includes a plurality of bottom panels and/or bottom flaps for forming a bottom wall of the carrier portion. For example, first major side panel 22 has a first bottom panel 38 extending therefrom along a fold line 40, first minor side panel 24 has a first bottom flap 42 extending therefrom along a fold line 44, second major side panel 26 has a second bottom panel 46 extending therefrom along a fold line 48, and second minor side panel 28 has a second bottom flap 50 extending therefrom along a fold line 52.
First blank 10 also includes a plurality of top panels and/or top flaps for forming a top wall of the carrier portion. For example, first major side panel 22 has a first top panel 54 extending therefrom along a fold line 56, first minor side panel 24 has a first top flap 58 extending therefrom along a fold line 60, second major side panel 26 has a second top panel 62 extending therefrom along a fold line 64, and second minor side panel 28 has a second top flap 66 extending therefrom along a fold line 68. Moreover, in one embodiment, first top panel 54 has a first handle panel 70 extending therefrom along a fold line 72, and second top panel 62 has a second handle panel 74 extending therefrom along a fold line 76. First handle panel 70 includes a handle cutout 78, and second handle panel 74 has a handle flap 80 defined therein by a partial cut line 82. As such, handle flap 80 remains coupled to second handle panel 74 along a fold line 84. One or more portions of handle panels 70 and 74 defining the respective cutouts may include features such as contours, grooves, and/or padding (e.g., gel-based, foam, or plastic) configured to provide a gripping surface.
In the example embodiment, first bottom panel 38 has a free edge 86 that defines a first locking tab 88, and second bottom panel 46 has a free edge 90 that defines a second locking tab 92. First and second locking tabs 88 and 92 facilitate forming an automatic bottom locking mechanism, which enables the container to be placed in a knocked-down flat position when bottom panels 38 and 46 move inside the cavity. More specifically, free edge 86 has a first angled edge portion 94, a first horizontal portion 96, and a second angled edge portion 98 that define a first locking notch 100. Similarly, free edge 90 has a third angled edge portion 102, a second horizontal portion 104, and a fourth angled edge portion 106 that define a second locking notch 108. As such, first locking tab 88 is sized for insertion within second locking notch 108, and second locking tab 92 is sized for insertion within first locking notch 100 when forming the bottom wall of the carrier portion. Alternatively, free edges 86 and 90 have any suitable configuration that enables blank 10 to function as described herein.
Carrier portion 200 is formed by folding first blank 10 along fold lines, perforation lines, and/or score lines. Specifically, side walls 202, 204, 206, and 208 are formed by rotating side panels 22, 24, 26, and 28 about fold lines 30, 32, 34, and 36. Joining tab 20 is then coupled to second minor side panel 28. Bottom wall 210 is formed by rotating bottom flaps 42 and 50 inwardly about fold lines 44 and 52, respectively, until bottom flaps 42 and 50 are substantially perpendicular to minor side panels 24 and 28. Bottom panels 38 and 46 are then rotated inwardly about fold lines 40 and 48, respectively, such that interior surfaces of bottom panels 38 and 46 couple to exterior surfaces 12 of bottom flaps 42 and 50. Moreover, first locking tab 88 is inserted within second locking notch 108, and second locking tab 92 is inserted within first locking notch 100 to form the bottom locking mechanism as bottom panels 38 and 46 are rotated inwardly.
Top wall 212 is formed by rotating top flaps 58 and 66 inwardly about fold lines 60 and 68, respectively, until top flaps 58 and 66 are substantially perpendicular to minor side panels 24 and 28. Top panels 54 and 62 are then rotated inwardly about fold lines 56 and 64, respectively, such that interior surfaces 14 of top panels 54 and 62 couple to exterior surfaces 12 of top flaps 58 and 66. More specifically, first top panel 54 is folded over second top panel 62 such that first handle panel 70 couples to second top panel 62. In one embodiment, first handle panel 70 is removably coupled to second top panel 62, e.g., with an adhesive and/or a hook and loop configuration to ensure carrier portion 200 remains in the shipping position during transport.
In some embodiments, shipping container portion 602 (shown in
In another embodiment, the patient can take a picture of an identifying marking associated with the medication dose that has been taken, and the picture can be transmitted to the server system via the patient application on the remote device. Alternatively, the patient application can have a user interface that enables the patient to manually input identifying information associated with the medication dose that has been taken. The identifying information can then be transmitted to the server system.
Referring again to
It should be understood that while discussed as standalone embodiments, features of the patient computing environment described above can be used either alone, or in combination, to facilitate monitoring patient compliance with a treatment regimen.
Second minor divider panel 322 extends from first minor divider panel 320 along fold line 330, third minor divider panel 324 extends from second minor divider panel 322 along fold line 332, fourth minor divider panel 326 extends from third minor divider panel 324 along fold line 334, and fifth minor divider panel 328 extends from fourth minor divider panel 326 along fold line 336. Fold lines 330, 332, 334, and 336 as well as other fold lines and/or hinge lines described herein, may include any suitable line of weakness and/or line of separation known to those skilled in the art and guided by the teachings herein provided.
In the example embodiment, a first cut line 338 is defined in second minor divider panel 322 to define a first securing tab 340 that extends from a first edge 342 of third minor divider panel 324, and a second cut line 344 is defined in fourth minor divider panel 326 to define a second securing tab 346 that extends from an opposing second edge 348 of third minor divider panel 324. First securing tab 340 has a first side edge 352, and second securing tab 346 has a second side edge 354. First securing tab 340 is positioned a first distance from a top edge 350 of second blank 300, and second securing tab 346 is positioned a greater second distance from top edge 350 than first securing tab 340. Moreover, first and second securing tabs 340 and 346 have a length L1 substantially equal to width W3 of first and fifth minor divider panels 320 and 328. As will be described in more detail below, securing tabs 340 and 346 and minor divider panels 320 and 328 at least partially define rectangular container slots, and having length L1 substantially equal to width W3 facilitates ensuring the internal divider insert remains securely positioned within carrier portion 200.
In one embodiment, a height of internal divider insert 400 is selected such that at least a portion of a carton positioned within one of the carton insertion slots protrudes beyond top edge 350. For example, internal divider insert 400 has a height such that a gap 508 is defined between top edge 350 and fold line 64 when internal divider insert 400 is coupled to bottom wall 210. As such, the height of internal divider insert 400 is selected to enable the portion of the carton protruding beyond top edge 350 to be easily grippable by a consumer.
Referring to
Moreover, carrier portion 200 is sized such that internal cavity 214 is capable of receiving one or more cartons 510 therein. As shown in
In the example embodiment, the materials and the dimensions of thermal insulation panels 606, 614, and 616 are selected to facilitate maintaining a temperature within thermally insulating cavity 608 within a predefined temperature range for a predetermined duration. More specifically, the materials and dimensions are selected such that the temperature within thermally insulating cavity 608 is maintained at a temperature below about 8° C. and, more specifically, within a range between about 8° C. and about 2° C., for a duration of at least about 48 hours to ensure the products contained within container portion 200 remain viable during shipping, for example.
For example, in one test run, container assembly 600 was formed and subjected to fluctuating ambient temperatures within a range between about 19° C. and about −5° C. for 48 hours. Over the course of the 48 hours, the temperature within thermally insulating cavity 608 was maintained within a range between about 8° C. and about 3° C. In another test run, container assembly 600 was formed and subjected to fluctuating ambient temperatures within a range between about 10° C. and about 31° C. for 48 hours. Over the course of the 48 hours, the temperature within thermally insulating cavity was maintained within a range between about 3° C. and about 7° C.
Second and third blanks 800 and 900 include a plurality of bottom panels and/or bottom flaps for forming a bottom wall of the carrier portion. For example, first major side panel 822 has a first bottom panel 838 extending therefrom, first minor side panel 824 has a first bottom flap 842 extending therefrom, second major side panel 826 has a second bottom panel 846 extending therefrom, and second minor side panel 828 has a second bottom flap 850 extending therefrom.
Second and third blanks 800 and 900 also include a plurality of top panels and/or top flaps for forming a top wall of the carrier portion. For example, first major side panel 822 has a first top panel 854 extending therefrom, first minor side panel 824 has a first top flap 858 extending therefrom, second major side panel 826 has a second top panel 862 extending therefrom, and second minor side panel 828 has a second top flap 866 extending therefrom. Moreover, in one embodiment, first top panel 854 has a first handle panel 870 extending therefrom, and second top panel 862 has a second handle panel 874 extending therefrom. Referring to
Blanks 800 and 900 form carrier portions sized to receive a single carton 510 therein, which enables internal divider insert 400 to be omitted from the carrier portion. As described above, the dimensions of blanks 800 and 900 are modified for receiving the single carton, as opposed to three cartons. For example, blanks 800 and 900 have substantially the same height as blank 10 (shown in
In the example embodiment, patient computing environment 1000 includes patient adherence system 218 and label/marking 220, which are associated with carrier portion 200 (shown in
As described above, patient adherence system 218 includes one or more labels/markings 220 that contain identifying data associated with each medication dose of the drug product shipped inside carrier portion 200. In one embodiment, label/marking 220 is a scannable marking such as, but not limited to, a quick response (QR) code and/or a bar code. In operation, the patient scans, with remote device 1004, the scannable label/marking 220 associated with a medication dose that is to be administered. The patient scans label/marking 220 each time the patient takes the medication dose. The QR code or the bar code contains data, such as the type of medication taken, or a lot or batch number of the medication taken. Patient application 1006 then transmits the data contained in the QR code or the bar code to server system 1008 for further analysis, as will be described in more detail below.
Alternatively, the patient can take a picture of an identifying marking associated with the medication dose that has been taken, and the picture can be transmitted to server system 1008 via patient application 1006 on remote device 1004. Alternatively, patient application 1006 can have a user interface that enables the patient to manually input identifying information associated with the medication dose that has been taken. The identifying information can then be transmitted to server system 1008.
The QR code or the bar code may also contain data relating to the patient that has taken the medication. The data may be de-identified data, which includes anonymized data that does not identify the particular patient for legal or other reasons, or may be identified data, which includes non-anonymized data that does identify the particular patient. For example, under national and/or regional patient privacy regulations such as the United States Health Insurance Portability and Accountability Act of 1996, only certain covered entities may be authorized to view identified patient protected health information (PHI) data.
Moreover, in some embodiments, server system 1008 may store user computing device identifiers, user identifiers, geographic identifiers associated with users, and transaction and shopping data associated with users, without including sensitive personal information, also known as personally identifiable information or PII, in order to ensure the privacy of individuals associated with the stored data. Personally identifiable information may include any information capable of identifying an individual. For privacy and security reasons, personally identifiable information may be withheld and only secondary identifiers may be used. For example, data received by server system 1008 may identify user “John Smith” as user “ZYX123” without any method of determining the actual name of user “ZYX123”. In some examples where privacy and security can otherwise be ensured (e.g., via encryption and storage security), or where individuals consent, personally identifiable information may be received and used by server system 1008. In such examples, personally identifiable information may be needed to reports about groups of users. In situations in which the systems discussed herein collect personal information about individuals, or may make use of such personal information, the individuals may be provided with an opportunity to control whether such information is collected or to control whether and/or how such information is used. In addition, certain data may be processed in one or more ways before it is stored or used, so that personally identifiable information is removed. For example, an individual's identity may be processed so that no personally identifiable information can be determined for the individual, or an individual's geographic location may be generalized where location data is obtained (such as to a city, ZIP code, or state level), so that a particular location of an individual cannot be determined.
Once label/marking 220 has been scanned, patient application 1006 transmits the data associated with label/marking 220 to server system 1008. In one embodiment, the patient application transmits additional information with the data, such as a time stamp of when the QR code or bar code was scanned (i.e., when the medication was taken). The combined data may then be stored or processed in server system 1008, and can be used for one or more purposes. For example, the data may be used to schedule reminders for the patient to administer future doses of the medication. In one embodiment, the reminders are sent to the patient and received at patient application 1006.
Alternatively or additionally, the combined data is stored or processed in server system 1008 for analysis to determine an effect of adherence to a specified treatment regimen on patient health outcomes. For example, in one embodiment, server system 1008 receives patient health outcome data for patient's taking the medication. Server system 1008 then analyzes the patient health outcome data (i.e., the patient's response to treatment), analyzes the adherence data (e.g., the type of medication taken and the timeliness of when medication taken), and determines the effect of adherence to or deviation from the specified treatment regimen. For example, if deviation from the specified treatment regimen results in an adverse patient health outcome, the data stored within server system 1008 can be used to form a remedial treatment regimen.
This written description uses examples to disclose various implementations, including the best mode, and also to enable any person skilled in the art to practice the various implementations, including making and using any devices or systems and performing any incorporated methods. The patentable scope of the disclosure is defined by the claims, and may include other examples that occur to those skilled in the art. Such other examples are intended to be within the scope of the claims if they have structural elements that do not differ from the literal language of the claims, or if they include equivalent structural elements with insubstantial differences from the literal language of the claims.
This application claims priority to U.S. Provisional Application No. 62/155,969 filed May 1, 2015, entitled “CONTAINER ASSEMBLY WITH AN INTERNAL DIVIDER AND METHOD OF FORMING THE SAME”, which is hereby incorporated by reference in its entirety.
Filing Document | Filing Date | Country | Kind |
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PCT/US2016/030011 | 4/29/2016 | WO | 00 |
Number | Date | Country | |
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62155969 | May 2015 | US |