Patent Application
20220261982
The present disclosure relates generally to the packaging of drug products, and, in particular, to methods, systems, and computer program products for validating drug product package contents based on characteristics of the drug product packaging system.
Drug product packaging systems may be used in facilities, such as pharmacies, hospitals, long term care facilities, and the like to dispense medications to fill prescriptions. These drug product packaging systems may include systems designed to package medications in various container types including, but not limited to, pouches, vials, bottles, blistercard, and strip packaging. Strip packaging is a type of packaging wherein medications are packaged in individual pouches for administration on a specific date and, in some cases, at a specific time. Typically, individual pouches are removably joined together and often provided in rolls. The pouches can be separated from the roll when needed.
Some types of drug product packages, such as pouches and blistercards, for example, may contain content printed thereon, such as Personal Health Information (PHI), manufacturer information, e.g., logos, names, contact information, etc., and/or other details about the content of the drug product package, such as number of drug products, drug product names, dosing times, dosing strengths, barcodes, and the like. Such content on the surface of the drug product package may make it more difficult to validate the content of the drug product package through imaging of the drug product package.
Moreover, different drug product packaging systems may have different characteristics with respect to the types of materials used in packaging the drug products and/or the validation system used in validating the contents of a drug product package. These variations between different drug product packaging systems may further complicate the evaluation of images taken of packaged drug products to confirm the contents thereof.
In some embodiments of the inventive concept, a method comprises, receiving an image of a drug product package that contains one or more drug products therein; detecting, using an artificial intelligence engine, characteristics of the image that are associated with a drug product packaging system; and generating a modified image of the drug product package based on characteristics of the drug product packaging system.
In other embodiments, the characteristics of the drug product packaging system comprise one or more image capture light source characteristics, one or more image capture surface characteristics, one or more packaging material characteristics, and/or one or more camera characteristics.
In still other embodiments, the one or more light source characteristics comprise strength of an image capture light source, intensity of the image capture light source, and/or location of the image capture light source.
In still other embodiments, the one or more image capture surface characteristics comprise background location and/or background color.
In still other embodiments, the one or more packaging material characteristics comprise packaging material transparency, packaging material shadow, labeling color, packaging material color, and/or packaging material hot spot.
In still other embodiments, the one or more camera characteristics comprise camera number, camera position, camera resolution, and/or camera image type.
In still other embodiments, the image is a first image, the drug product package is a first drug product package, and the modified image is a first modified image. Detecting, using the artificial intelligence engine, the characteristics of the first image comprises detecting, using the artificial intelligence engine, characteristics of the first image that are associated with a first one of a plurality of drug product packaging systems. Generating the first modified image comprises generating the first modified image of the first drug product package based on characteristics of the first one of the plurality of drug product packaging systems.
In still other embodiments, the method further comprises receiving a second image of a second drug product package that contains one or more drug products therein; detecting, using the artificial intelligence engine, characteristics of the second image that are associated with a second one of the plurality of drug product packaging systems; and generating a second modified image of the second drug product package based on characteristics of the second one of the plurality of drug product packaging systems.
In still other embodiments, the method further comprises detecting, using an artificial intelligence engine, labeling content on a surface of the drug product package. Generating the modified image of the drug product package comprises generating a modified image of the drug product package that has the labeling content removed from the surface thereof.
In still other embodiments, the artificial intelligence engine is a first artificial intelligence engine and the modified image is a first modified image. The method further comprises receiving order information for the one or more drug products and an identifier for the drug product package; detecting, using a second artificial intelligence engine, individual ones of the one or more drug products in the first modified image; and generating a second modified image of the drug product package that includes indicia that distinguish between the individual ones of the one or more drug products and associate the one or more drug products with the order information and the identifier for the drug product package.
In still other embodiments, the order information comprises names for the one or more drug products in the drug product package. The method further comprises identifying, using a third artificial intelligence engine, at least some of the one or more drug products in the second modified image based on the names for the one or more drug products. The names are associated with drug product attributes in a reference database.
In still other embodiments, the method further comprises performing gamma correction on the image of the drug product package responsive to receiving the image of the drug product package to generate a gamma corrected image of the drug product package; performing gaussian blur denoising on the gamma corrected image of the drug product package to generate a reduced noise image of the drug product package; and performing automatic image thresholding on the reduced noise image of the drug product package to generate a foreground-background separated image of the drug product package. Detecting, using the artificial intelligence engine, the labeling content comprises detecting, using the artificial intelligence engine, the labeling content on the surface of the foreground-background separated image of the drug product package.
In some embodiments of the inventive concept, a system comprises a processor and a memory coupled to the processor and comprising computer readable program code embodied in the memory that is executable by the processor to perform operations comprising: receiving an image of a drug product package that contains one or more drug products therein; detecting, using an artificial intelligence engine, characteristics of the image that are associated with a drug product packaging system; and generating a modified image of the drug product package based on characteristics of the drug product packaging system.
In further embodiments, the characteristics of the drug product packaging system comprise one or more image capture light source characteristics, one or more image capture surface characteristics, one or more packaging material characteristics, and/or one or more camera characteristics.
In still further embodiments, the one or more light source characteristics comprise strength of an image capture light source, intensity of the image capture light source, and/or location of the image capture light source.
In still further embodiments, the one or more image capture surface characteristics comprise background location and/or background color.
In still further embodiments, the one or more packaging material characteristics comprise packaging material transparency, packaging material shadow, labeling color, packaging material color, and/or packaging material hot spot.
In still further embodiments, the one or more camera characteristics comprise camera number, camera position, camera resolution, and/or camera image type.
In still further embodiments, the image is a first image, the drug product package is a first drug product package, and the modified image is a first modified image. Detecting, using the artificial intelligence engine, the characteristics of the first image comprises detecting, using the artificial intelligence engine, characteristics of the first image that are associated with a first one of a plurality of drug product packaging systems. Generating the first modified image comprises generating the first modified image of the first drug product package based on characteristics of the first one of the plurality of drug product packaging systems.
In still further embodiments, the operations further comprise receiving a second image of a second drug product package that contains one or more drug products therein; detecting, using the artificial intelligence engine, characteristics of the second image that are associated with a second one of the plurality of drug product packaging systems; and generating a second modified image of the second drug product package based on characteristics of the second one of the plurality of drug product packaging systems.
In some embodiments of the inventive concept, a computer program product comprises a non-transitory computer readable storage medium comprising computer readable program code embodied in the medium that is executable by a processor to perform operations comprising: receiving an image of a drug product package that contains one or more drug products therein; detecting, using an artificial intelligence engine, characteristics of the image that are associated with a drug product packaging system; and generating a modified image of the drug product package based on characteristics of the drug product packaging system.
Other methods, systems, articles of manufacture, and/or computer program products according to embodiments of the inventive concept will be or become apparent to one with skill in the art upon review of the following drawings and detailed description. It is intended that all such additional systems, methods, articles of manufacture, and/or computer program products be included within this description, be within the scope of the present inventive subject matter and be protected by the accompanying claims.
Other features of embodiments will be more readily understood from the following detailed description of specific embodiments thereof when read in conjunction with the accompanying drawings, in which:
In the following detailed description, numerous specific details are set forth to provide a thorough understanding of embodiments of the present inventive concept. However, it will be understood by those skilled in the art that the present invention may be practiced without these specific details. In some instances, well-known methods, procedures, components, and circuits have not been described in detail so as not to obscure the present inventive concept. It is intended that all embodiments disclosed herein can be implemented separately or combined in any way and/or combination. Aspects described with respect to one embodiment may be incorporated in different embodiments although not specifically described relative thereto. That is, all embodiments and/or features of any embodiments can be combined in any way and/or combination.
As used herein, the term “data processing facility” includes, but it is not limited to, a hardware element, firmware component, and/or software component. A data processing system may be configured with one or more data processing facilities.
The term “drug product packaging system,” as used herein, refers to any type of pharmaceutical dispensing system including, but not limited to, automated systems that fill vials, bottles, containers, pouches, blistercards, or the like with drug product, semi-automated systems that fill vials, bottles, containers, pouches, blistercards, or the like with drug product, and any combination of automated and semi-automated systems for filling a drug product package with drug product. Drug product packaging system also includes packaging systems for pharmaceutical alternatives, such as nutraceuticals and/or bioceuticals.
The terms “pharmaceutical” and “medication,” as used herein, are interchangeable and refer to medicaments prescribed to patients either human or animal. A pharmaceutical or medication may be embodied in a variety of ways including, but not limited to, pill form capsule form, tablet form, and the like.
The term “drug product” refers to any type of medicament that can be packaged within a vial, bottle, container, pouch, blistercard, or the like by automated and semi-automated drug product packaging systems including, but not limited to, pills, capsules, tablets, caplets, gel caps, lozenges, and the like. Drug product also refers to pharmaceutical alternatives, such as nutraceuticals and/or bioceuticals. Example drug product packaging systems including management techniques for fulfilling packaging orders are described in U.S. Pat. No. 10,492,987 the disclosure of which is hereby incorporated herein by reference.
The term “drug product package” refers to any type of object that can hold a drug product including, but not limited to, a vial, bottle, container, pouch, blistercard, or the like.
The term “National Drug Code (NDC)” may be used to represent both NDC information and “Drug Identification Number (DIN)” information.
Embodiments of the inventive concept are described herein in the context of a drug product packaging analysis engine that includes one or more machine learning engines and artificial intelligence (AI) engines. It will be understood that embodiments of the inventive concept are not limited to particular implementations of the drug product analysis engine and various types of AI systems may be used including, but not limited to, a multi-layer neural network, a deep learning system, a natural language processing system, and/or computer vision system Moreover, it will be understood that the multi-layer neural network is a multi-layer artificial neural network comprising artificial neurons or nodes and does not include a biological neural network comprising real biological neurons. Embodiments of the inventive concept may be implemented using multiple AI systems or may be implemented by combining various functionalities into fewer or a single AI system.
Some embodiments of the inventive concept stem from a realization that when validating the contents of a drug product package, such as a pouch or blistercard, for example, different drug product packaging systems may have different characteristics that can affect the validation process due to, for example, differences in the physical packaging being used as well as the image capture system used by the different drug product packaging systems to capture images of the drug product packages. For example, the characteristics of the drug product packaging system may comprise one or more image capture light source characteristics, one or more image capture surface characteristics, one or more packaging material characteristics, and/or one or more camera characteristics. The one or more light source characteristics may comprise, for example, strength of an image capture light source, intensity of the image capture light source, and/or location of the image capture light source. Ambient light may also affect the light source characteristics based on the construction of the image capture system associated with the drug product packaging system. The one or more image capture surface characteristics may comprise background location and/or background color. The one or more packaging material characteristics may comprise packaging material transparency, packaging material shadow, labeling color, packaging material color, and/or packaging material hot spot. Colors may be used on a drug product package to differentiate drug product and each color may represent a different drug class. For example, blue labels may be used to identify opioids, fluorescent red may be used to identify neuromuscular blockers, yellow may be used to identify induction agents, orange may be used to identify tranquilizers, violet may be used to identify vasopressors, and green may be used to identify anticholinergics. Blue vials may be used to identify drug products that need to be kept out of reach of children. Blue pill bottles may be made from polyethylene material that is generally long lasting. The pill bottles may secure different quantities and sizes of drug products for safe transport and storage. Pill bottles may be translucent orange to mimic amber colored bottles that were used historically. The orange coloring may reduce damage to the drug products contained therein due to UV light. The one or more camera characteristics comprise camera number, camera position, camera resolution, and/or camera image type. Profile information including the above-described characteristics may be stored for each of the drug product packaging systems to aid in drug product packaging system specific image recognition. The profile information for each drug product packaging system may not be static and may evolve over time due to changes in the external environment, parts changes/wear, and the like. Thus, as the drug product packaging system's characteristics evolve, the AI system may likewise be trained to recognize the evolving characteristics over time. Conventional drug product package content validation systems are typically tailored to a particular drug product packaging system. By taking into account variations in the packaging and/or the image capture system used in different drug product packaging systems in validating the contents of the drug product packages through use of an AI system, the accuracy of the drug product packaging validation can be improved. Moreover, the drug product package content validation may be moved in whole or in part into a network location, such as the cloud, allowing a pharmacy or other drug product packaging facility to access the AI based drug product package validation system that has been trained on multiple types of drug product packaging systems. As new drug product packaging systems are developed, the AI system may be trained to recognize the particular characteristics of the new drug product packaging system. In other embodiments, some facilities may desire to run the drug product package content validation locally rather than over a network, such as via the cloud. In other embodiments, the AI system may be modified to run locally at a particular pharmacy or drug product packaging facility and may be pared down to support the particular drug product packaging system used at that pharmacy or facility without supporting other drug product packaging systems.
Referring to
The PMS system 110 may be configured to manage and fill prescriptions for customers. As used herein, PMS systems may be used in pharmacies or may be used generally as batch-generating systems for other applications, such as dispensing nutraceuticals or bioceuticals. The PMS system 110 may be associated with a variety of types of facilities, such as pharmacies, hospitals, long term care facilities, and the like. The PMS system or host system 110 may be any system capable of sending a valid prescription to the one or more product packaging systems 130a and 130b. The packaging system server 120 may include a packaging system interface module 135 and may be configured to manage the operation of the drug product packaging systems 130a and 130b. For example, the packaging system server 120 may be configured to receive packaging orders from the PMS system 110 and to identify which of the drug product packaging systems 130a and 130b should be used to package particular individual orders or batches of orders. In some embodiments, an AI system may be used to facilitate intelligent routing of drug product packaging orders to specific drug product packaging systems as described, for example, in U.S. patent application Ser. No. 17/510,635, filed Oct. 26, 2021 entitled ORGANIZATION OF SCRIPT PACKAGING SEQUENCE AND PACKAGING SYSTEM SELECTION FOR DRUG PRODUCTS USING AN ARTIFICIAL INTELLIGENCE ENGINE, the content of which is incorporated herein by reference.
In addition, the packaging system server 120 may be configured to manage the operations of the drug product packaging systems 130a and 130b. For example, the packaging system server 120 may be configured to manage the inventory of drug product available through each of the drug product packaging systems 130a and 130b, to manage the drug product dispensing canisters assigned or registered to one or more of the drug product packaging systems 130a and 130b, to manage the operational status generally of the drug product packaging systems 130a and 130b, and/or to manage reports regarding the status (e.g., assignment, completion, etc.) of packaging orders, drug product inventory, order billing, and the like. A user 150, such as a pharmacist or pharmacy technician, may communicate with the packaging system server 120 using any suitable computing device via a wired and/or wireless connection. Although the user 150 is shown communicating with the packaging system server 120 via a direct connection in
The AI assisted drug product package analysis system may include the package analysis engine(s) servers 155A and/or 155B, which includes package analysis engine(s) modules 160A and 160B to facilitate validation of the contents of a drug product package while taking into account variations between characteristics of the different drug product packaging systems 130a and 130b. In accordance with various embodiments of the inventive concept, the drug product package analysis service may be provided over a network connection, such as a cloud service, by way of the package engine analysis engine server 155B and the package analysis engine module 160B and/or may be provided locally, for example, at a pharmacy or drug product packaging facility by way of the package engine analysis engine server 155A and the package analysis engine module 160A. As will be described herein, the AI assisted drug product package analysis service may be provided as a composite service in which an AI system is trained to account for multiple types of drug product packaging systems or may be provided as a targeted service to account for a single type of drug product packaging system. A pharmacy or other drug product packaging facility may wish to run the AI assisted drug product package analysis service locally, which is targeted to a specific drug product packaging system used in the pharmacy or facility. In other embodiments, a pharmacy or drug product packaging facility may wish to access the drug product package analysis service as a cloud service, in which the AI system is trained to account for the varying characteristics of multiple types of drug product packaging systems as the pharmacy or drug product packaging facility may use multiple types of drug product packaging systems or may not wish to setup the resources locally to run the drug product package analysis service. The package engine analysis engine server 155B and the package analysis engine module 160B along with the package engine analysis engine server 155A and the package analysis engine module 160A will be collectively referred to herein as the package analysis engine server 155 and the package analysis engine module 160. The package analysis engine server 155 and the package analysis engine module 160 may facilitate AI assisted drug product package analysis to validate the drug product package contents while accounting for variations in characteristics of drug product packaging systems for drug product packaging systems in a same physical locations and across multiple physical locations.
The package analysis engine(s) server 155 and package analysis engine(s) module 160 may represent one or more AI systems that may be configured to generate a modified image of a drug product package based on the characteristics of the drug product packaging system, to generate modified images of drug product packages with labeling content removed from one or more surfaces thereof, to detect in a drug product package image individual ones of one or more drug products contained in the drug product package, and/or to identify these drug products that have been detected in the drug product package image. In accordance with some embodiments of the inventive concept, the characteristics of the drug product packaging system may comprise one or more image capture light source characteristics, one or more image capture surface characteristics, one or more packaging material characteristics, and/or one or more camera characteristics. In accordance with various embodiments of the inventive concept, the labeling content can be removed from any surface on the drug product package including multiple surfaces of the drug product package, such as the top, bottom, and sides of vials, front and back surfaces of pouches and blister packs, and the like.
It will be understood that the division of functionality described herein between the packaging system server 120/packaging system interface module 135 and the package analysis engine(s) server 155/package analysis engine(s) module 160 is an example. Various functionality and capabilities can be moved between the packaging system server 120/packaging system interface module 135 and the package analysis engine(s) server 155/package analysis engine(s) module 160 in accordance with different embodiments of the inventive concept. Moreover, in some embodiments, the packaging system server 120/packaging system interface module 135 and the package analysis engine(s) server 155/package analysis engine(s) module 160 may be merged as a single logical and/or physical entity.
A network 140 couples the drug product packaging systems 130a and 130b, the PMS system 110, the package engine analysis engine server 155B, and the packaging system server 120 to one another. The network 140 may be a global network, such as the Internet or other publicly accessible network. Various elements of the network 140 may be interconnected by a wide area network, a local area network, an Intranet, and/or other private network, which may not be accessible by the general public. Thus, the communication network 140 may represent a combination of public and private networks or a virtual private network (VPN). The network 140 may be a wireless network, a wireline network, or may be a combination of both wireless and wireline networks. In some embodiments, the package analysis engine(s) server 155 may also be coupled to the network 140.
The AI assisted drug product package analysis service provided through the package analysis engine(s) server 155, and package analysis engine(s) module 160, in some embodiments, may be implemented as a cloud service, such as through the package engine analysis engine server 155B and the package analysis engine module 160B. In some embodiments, the AI assisted drug product package analysis service may be implemented as a Representational State Transfer Web Service (RESTful Web service).
Although
As described above, the package analysis engine(s) server 155 and package analysis engine(s) module 160 may represent one or more AI systems that may be configured to account for variations between different drug product packaging systems, to generate modified images of drug product packages with labeling content removed from the surfaces thereof, to detect in a drug product package image individual ones of one or more drug products contained in the drug product package, and/or to identify these drug products that have been detected in the drug product package image.
The training data 205 may comprise one or more images of a drug product package that each contain one or more drug products therein. The drug product package(s) may include labeling content on a surface thereof, which may include, but is not limited to, commercial marketing information, patient identification information and/or personal healthcare information (PHI). The commercial marketing information may include, for example, a logo and/or a business name. The patient identification information may include, for example, a patient name, a patient phone number, a patient address, and/or a patient identification number. The personal health care information may include, for example, names of the one or more drug products contained in the drug product package, a time of administration for each of the one or more drug products, one or more barcodes associated with the one or more drug products, a prescription order, a patient account, an identification number, and/or other information. In some embodiments, the drug product package image may be modified, such that at least a portion of the labeling content contained on the surface thereof is removed through use of an AI system, such as a neural network, described below with reference to
The featuring module 225 is configured to identify the individual independent variables that are used by the package analysis engine(s) module 160 to detect and/or identify one or more drug products in, for example, a drug product package image having had the labeling content removed, which may be considered dependent variable(s), while accounting for the characteristics of the drug product packaging system used in packaging the one or more drug products. For example, the training data 205 may be generally unprocessed or formatted and include extra information in addition to drug product and/or drug product packaging information. For example, the training data 205 may include account codes, business address information, and the like, which can be filtered out by the featuring module 225. The features extracted from the training data 205 may be called attributes and the number of features may be called the dimension. The labeling module 230 may be configured to assign defined labels to the training data and to the detected and/or identified drug products to ensure a consistent naming convention for both the input features and the generated outputs. The machine learning engine 240 may process both the featured training data 205, including the labels provided by the labeling module 230, and may be configured to test numerous functions to establish a quantitative relationship between the featured and labeled input data and the generated outputs. The machine learning engine 240 may use modeling techniques to evaluate the effects of various input data features on the generated outputs. These effects may then be used to tune and refine the quantitative relationship between the featured and labeled input data and the generated outputs. The tuned and refined quantitative relationship between the featured and labeled input data generated by the machine learning engine 240 is output for use in the AI engine 245. The machine learning engine 240 may be referred to as a machine learning algorithm. As shown in
The modules used to detect in a drug product package image individual ones of one or more drug products contained in the drug product package and/or to identify these drug products that have been detected in the drug product package image based on the characteristics of the drug product packaging system used to generate the drug product package include the new data module 255, the featuring module 265, the AI engine module 245, and the drug product package processing and analysis module 275. The new data 255 may be the same data/information as the training data 205 in content and form except the new data 255 will be used for an analysis of a new drug product package rather than for training purposes. Likewise, the featuring module 265 performs the same functionality on the new data 255 as the featuring module 225 performs on the training data 205. The AI engine 245 may, in effect, be generated by the machine learning engine 240 in the form of the quantitative relationship determined between the featured and labeled input data and the output drug product package content analysis. The AI engine 245 may, in some embodiments, be referred to as an AI model. Similar to the machine learning engine 240, the AI engine 245 supports multiple individual packaging systems as represented by the packaging system A module 247A and the packaging system B module 247B. The machine learning engine 240 may further support the analysis of drug product package images from one or more of a plurality of packaging systems as represented by the composite packaging system module 247C. The AI engine 245 may be configured to generate modified images of a drug product package that includes indicia that distinguish between individual ones of the one or more drug products contained therein while associating the one or more drug products with order information and/or an identifier for the drug product package based on characteristics of the drug product packaging system used to package the one or more drug products. The indicia may be embodied in a variety of ways including, but not limited to, boundary boxes or polygons, circles, an enclosed shape that includes straight and curved surfaces, an enclosed shape that includes only curved surfaces, and/or lines or symbols that demarcate boundaries between the one or more drug products. In some embodiments, the indicia may take a shape that approximates the shape of the drug product. The AI engine 245 may also be configured to identify one or more of the drug products based on their names. The AI engine 245 may use a variety of modeling techniques to detect in a drug product package image individual ones of one or more drug products contained in the drug product package and to identify these drug products that have been detected in the drug product package image based on the characteristics of the drug product packaging system used to package the one or more drug products in accordance with different embodiments of the inventive concept including, but not limited to, a regression technique, a neural network technique, an Autoregressive Integrated Moving Average (ARIMA) technique, a deep learning technique, a linear discriminant analysis technique, a decision tree technique, a naïve Bayes technique, a K-nearest neighbors technique, a learning vector quantization technique, a support vector machine technique, and/or a bagging/random forest technique.
The drug product package processing and analysis module 275 may be configured to output the modified drug product package image with the one or more drug products identified by way of indicial, such as boundary boxes, along with names for the one or more drug products to a drug product package validation system.
As described above, the package analysis engine(s) server 155 and package analysis engine(s) module 160 may represent one or more AI systems that may be configured to generate modified images of drug product packages with labeling content removed from the surfaces thereof based on characteristics of the drug product packaging system used in the packaging.
Referring now to
In some embodiments of the inventive concept, the multi-packaging system convolutional neural network 310 may be a residual neural network in which skip connections are used between the convolutional layers 320 and 330. An example of the skip connection is shown in
It will be understood that while two convolutional layers 320 and 330 are shown in in the example multi-packaging system convolutional neural network 310 of
As described above, embodiments of the inventive concept may provide an AI assisted drug product package analysis system that can be used to account for variations between different drug product packaging systems through the composite packaging system module 242C, the composite packaging system module 247C and the multi-packaging system convolutional neural network 310. Thus, embodiments of the inventive concept may be used to process images of drug product packages from different drug product packaging systems and generate respective modified images that are based on the characteristics of the different drug product packaging systems, respectively. Referring now to
Embodiments of the inventive concept may provide one or more AI systems that may facilitate the validation of the contents of a drug product package by generating a modified image of a drug product package based on the characteristics of the drug product packaging system, generating modified images of drug product packages with labeling content removed from one or more surfaces thereof, detecting in a drug product package image individual ones of one or more drug products contained in the drug product package, and/or identifying these drug products that have been detected in the drug product package image. The accuracy of embodiments for validating the contents of drug product packages in which labeling content has been at least partially removed including detecting individual ones of one or more drug products in the package and identifying these identified drug products by name may be further improved through taking into account the particular characteristics of the drug product packaging systems used to package the drug products when analyzing the drug product package images. Embodiments for generating modified images of drug product packages with labeling content removed from one or more surfaces thereof, detecting in a drug product package image individual ones of one or more drug products contained in the drug product package, and/or identifying these drug products that have been detected in the drug product package image are described below and in U.S. patent application Ser. No. 17/649,208 entitled “METHODS, SYSTEMS, AND COMPUTER PROGRAM PRODUCT FOR REMOVING EXTRANEOUS CONTENT FROM DRUG PRODUCT PACKAGING TO FACILITATE VALIDATION OF THE CONTENTS THEREIN,” filed Jan. 28, 2022, the content of which is hereby incorporated herein by reference.
Referring now to
As described above, the drug product package image may undergo pre-processing to perform various corrections to the image data. Referring now to
Referring now to
Referring now to
According to some embodiments of the inventive concept, the operations described above with respect to
Referring now to
Although
Computer program code for carrying out operations of data processing systems discussed above with respect to
Moreover, the functionality of the drug product package analysis engine(s) server 155 of
The data processing apparatus described herein with respect to
As described above, embodiments of the inventive concept may provide an AI assisted drug product package analysis system that may use AI technology, such as a convolutional neural network to validate the contents of a drug product package, such as a pouch or blistercard, for example, while accounting for variations in characteristics of different drug product packaging systems, which may affect the validation process due to, for example, differences in the physical packaging being used as well as the image capture system used by the different drug product packaging systems to capture images of the drug product packages. According to some embodiments of the inventive concept, the AI system may be trained to account for differences in drug product packaging system characteristics while modifying images of drug product packages to facilitate the validation of the contents contained therein. For example, AI systems according to some embodiments of the inventive concept may use a convolutional neural network to detect the labeling content on the surface of a drug product package to generate a modified image of the drug product package with the labeling content removed and one or more machine learning engines to detect and identify the drug products contained in the drug product package. this may improve the accuracy of the package validation process before, for example, a pharmacy or medical center releases packaged drug products to a customer or patient.
In the above-description of various embodiments of the present disclosure, aspects of the present disclosure may be illustrated and described herein in any of a number of patentable classes or contexts including any new and useful process, machine, manufacture, or composition of matter, or any new and useful improvement thereof. Accordingly, aspects of the present disclosure may be implemented entirely hardware, entirely software (including firmware, resident software, micro-code, etc.) or combining software and hardware implementation that may all generally be referred to herein as a “circuit,” “module,” “component,” or “system.” Furthermore, aspects of the present disclosure may take the form of a computer program product comprising one or more computer readable media having computer readable program code embodied thereon.
Any combination of one or more computer readable media may be used. The computer readable media may be a computer readable signal medium or a computer readable storage medium. A computer readable storage medium may be, for example, but not limited to, an electronic, magnetic, optical, electromagnetic, or semiconductor system, apparatus, or device, or any suitable combination of the foregoing. More specific examples (a non-exhaustive list) of the computer readable storage medium would include the following: a portable computer diskette, a hard disk, a random access memory (RAM), a read-only memory (ROM), an erasable programmable read-only memory (EPROM or Flash memory), an appropriate optical fiber with a repeater, a portable compact disc read-only memory (CD-ROM), an optical storage device, a magnetic storage device, or any suitable combination of the foregoing. In the context of this document, a computer readable storage medium may be any tangible medium that can contain or store a program for use by or in connection with an instruction execution system, apparatus, or device.
A computer readable signal medium may include a propagated data signal with computer readable program code embodied therein, for example, in baseband or as part of a carrier wave. Such a propagated signal may take any of a variety of forms, including, but not limited to, electro-magnetic, optical, or any suitable combination thereof. A computer readable signal medium may be any computer readable medium that is not a computer readable storage medium and that can communicate, propagate, or transport a program for use by or in connection with an instruction execution system, apparatus, or device. Program code embodied on a computer readable signal medium may be transmitted using any appropriate medium, including but not limited to wireless, wireline, optical fiber cable, RF, etc., or any suitable combination of the foregoing.
Computer program code for carrying out operations for aspects of the present disclosure may be written in any combination of one or more programming languages, including an object oriented programming language such as Java, Scala, Smalltalk, Eiffel, JADE, Emerald, C++, C#, VB.NET, Python or the like, conventional procedural programming languages, such as the “C” programming language, Visual Basic, Fortran 2003, Perl, COBOL 2002, PHP, ABAP, dynamic programming languages such as Python, Ruby and Groovy, or other programming languages. The program code may execute entirely on the user's computer, partly on the user's computer, as a stand-alone software package, partly on the user's computer and partly on a remote computer or entirely on the remote computer or server. In the latter scenario, the remote computer may be connected to the user's computer through any type of network, including a local area network (LAN) or a wide area network (WAN), or the connection may be made to an external computer (for example, through the Internet using an Internet Service Provider) or in a cloud computing environment or offered as a service such as a Software as a Service (SaaS).
Aspects of the present disclosure are described herein with reference to flowchart illustrations and/or block diagrams of methods, apparatus (systems), and computer program products according to embodiments of the disclosure. It will be understood that each block of the flowchart illustrations and/or block diagrams, and combinations of blocks in the flowchart illustrations and/or block diagrams, can be implemented by computer program instructions. These computer program instructions may be provided to a processor of a general purpose computer, special purpose computer, or other programmable data processing apparatus to produce a machine, such that the instructions, which execute via the processor of the computer or other programmable instruction execution apparatus, create a mechanism for implementing the functions/acts specified in the flowchart and/or block diagram block or blocks.
These computer program instructions may also be stored in a computer readable medium that when executed can direct a computer, other programmable data processing apparatus, or other devices to function in a particular manner, such that the instructions when stored in the computer readable medium produce an article of manufacture including instructions which when executed, cause a computer to implement the function/act specified in the flowchart and/or block diagram block or blocks. The computer program instructions may also be loaded onto a computer, other programmable instruction execution apparatus, or other devices to cause a series of operational steps to be performed on the computer, other programmable apparatuses or other devices to produce a computer implemented process such that the instructions which execute on the computer or other programmable apparatus provide processes for implementing the functions/acts specified in the flowchart and/or block diagram block or blocks.
The flowchart and block diagrams in the figures illustrate the architecture, functionality, and operation of possible implementations of systems, methods, and computer program products according to various aspects of the present disclosure. In this regard, each block in the flowchart or block diagrams may represent a module, segment, or portion of code, which comprises one or more executable instructions for implementing the specified logical function(s). It should also be noted that, in some alternative implementations, the functions noted in the block may occur out of the order noted in the figures. For example, two blocks shown in succession may, in fact, be executed substantially concurrently, or the blocks may sometimes be executed in the reverse order, depending upon the functionality involved. It will also be noted that each block of the block diagrams and/or flowchart illustration, and combinations of blocks in the block diagrams and/or flowchart illustration, can be implemented by special purpose hardware-based systems that perform the specified functions or acts, or combinations of special purpose hardware and computer instructions.
The terminology used herein is for the purpose of describing particular aspects only and is not intended to be limiting of the disclosure. As used herein, the singular forms “a”, “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms “comprises,” “comprising,” “include”, “including”, “includes”, “have”, “has”, “having”, or variants thereof when used in this specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof. As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items. Like reference numbers signify like elements throughout the description of the figures.
It will also be understood that, although the terms first, second, etc. may be used herein to describe various elements, these elements should not be limited by these terms. These terms are only used to distinguish one element from another.
Unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the specification and relevant art and should not be interpreted in an idealized or overly formal sense unless expressly so defined herein. Well-known functions or constructions may not be described in detail for brevity and/or clarity.
The description of the present disclosure has been presented for purposes of illustration and description, but is not intended to be exhaustive or limited to the disclosure in the form disclosed. Many modifications and variations will be apparent to those of ordinary skill in the art without departing from the scope and spirit of the disclosure. The aspects of the disclosure herein were chosen and described in order to best explain the principles of the disclosure and the practical application, and to enable others of ordinary skill in the art to understand the disclosure with various modifications as are suited to the particular use contemplated.
The present application claims priority from and the benefit of U.S. Provisional Application No. 63/150,820, filed Feb. 18, 2021, the disclosure of which is hereby incorporated herein by reference in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| 63150820 | Feb 2021 | US |
