Pathological reagent quality control information management method and system, electronic equipment and medium

Abstract

The invention provides a quality control information management method and system of a pathological reagent, electronic equipment and a medium. The method comprises the following steps: acquiring reagent information recorded in a first reagent label of a reagent in and out of a warehouse; acquiring quality control information obtained by performing batch-to-batch quality control experiments on the reagent; generating a second reagent label recording all or part of the reagent information and the quality control information; the second reagent label is used for identifying the reagent subjected to the batch-to-batch quality control experiment. According to the method, the new reagent label (the second reagent label) can be automatically generated, the standard management of the quality control information of the reagent is realized, the manual copying link is reduced, the working efficiency and the correct rate of recording can be improved, the recording standardization is realized, and the traceability of reagent use is enhanced.

Description

Technical Field

[0001] The present disclosure relates to the technical field of material management, and particularly to a quality control information management method, system, electronic device, and medium for pathological reagents. Background Art

[0002] The detection antibodies used for immunohistochemistry in pathological diagnosis are all commercial reagents, which vary due to different reagent manufacturers, clone numbers, etc. Even for the same manufacturer, there are batch-to-batch differences between different batch numbers. Reagents without sufficient comparison may have a variation rate of up to 20% between different batches, which has a significant impact on experimental results. Therefore, when replacing the clinical detection antibodies with new batch numbers, batch-to-batch quality control must be carried out, and only the reagents with qualified quality control can be used for clinical detection.

[0003] Currently, in the industry, batch-to-batch quality control mainly relies on manual registration of reagent incoming and outgoing, and manually matching the old and new batch numbers according to the reagent activation date, including printing labels, marking label information, printing comparison tables and slides, pathological technicians performing experimental operations, pathological doctors making diagnostic interpretations and experimental records, and archiving quality control slides, etc. This process mainly relies on experienced technicians to operate, and the records are cumbersome and error-prone. Summary of the Invention

[0004] The technical problem to be solved by the present disclosure is to overcome the above-mentioned defects in the prior art and provide a quality control information management method, system, electronic device, and medium for pathological reagents.

[0005] The present disclosure solves the above technical problems through the following technical solutions:

[0006] In a first aspect, a quality control information management method for reagents is provided, including:

[0007] Obtaining reagent information recorded in a first reagent label of the incoming and outgoing reagents;

[0008] Obtaining quality control information obtained from batch-to-batch quality control experiments on the reagents;

[0009] Generating a second reagent label recording all or part of the reagent information and the quality control information; the second reagent label is a new label received for storage.

[0010] Optionally, obtaining quality control information obtained from batch-to-batch quality control of the reagents includes:

[0011] Responding to a quality control information entry instruction, and displaying a first information entry template matching the quality control information entry instruction;

[0012] Obtaining quality control data filled in the first information entry template, and generating the quality control information according to the first information entry template.

[0013] Optionally, the first reagent label is a barcode provided on the carrier assembly of the reagent; obtaining the reagent information recorded in the first reagent label of the incoming and outgoing reagents, including:

[0014] Scanning the barcode to obtain initial information, and extracting the target parameters included in the initial information using a second information entry template to obtain reagent information including the target parameters; wherein, the incoming library template includes fields corresponding to the target parameters.

[0015] Optionally, both the reagent information and the quality control information include the batch number of the reagent; the quality control information management method further includes:

[0016] Associating and storing the reagent information and the quality control information in a database according to the batch number.

[0017] Optionally, it further includes:

[0018] In response to a comparison instruction for a target batch, extracting the quality control information obtained from the quality control experiment between batches that matches the target batch from the database to compare the quality control results.

[0019] Optionally, it further includes:

[0020] Sending the second reagent label to a printer for printing;

[0021] And / or, transcribing the quality control information into a table according to a set quality control template and printing it.

[0022] In a second aspect, a quality control information management system for reagents is provided, including:

[0023] A first acquisition module, configured to acquire the reagent information recorded in the first reagent label of the incoming and outgoing reagents;

[0024] A second acquisition module, configured to acquire the quality control information obtained from the between-batch quality control experiment on the reagent;

[0025] A generation module, configured to generate a second reagent label recording all or part of the reagent information and the quality control information; the second reagent label is a newly received incoming library label.

[0026] In a third aspect, an electronic device is provided, including a memory, a processor, and a computer program stored on the memory and configured to run on the processor, where when the processor executes the computer program, the quality control information management method for pathological reagents described in any item of the first aspect is implemented.

[0027] Fourthly, a computer-readable storage medium is provided, on which a computer program is stored. It is characterized in that when the computer program is executed by a processor, the quality control information management method of the pathological reagent described in any one of the first aspects is implemented.

[0028] Fifthly, a computer program product is provided, including a computer program, and when the computer program is executed by a processor, the quality control information management method of the pathological reagent described in any one of the first aspects is implemented.

[0029] On the basis of conforming to common general knowledge in the art, the above-mentioned preferred conditions can be combined arbitrarily to obtain various preferred examples of the present disclosure.

[0030] The positive and progressive effects of the present disclosure are as follows: The present disclosure can automatically generate a new reagent label (the second reagent label), realize the standardized management of the quality control information of the reagent, reduce the manual transcription link, improve the work efficiency and the accuracy rate of records, realize the record standardization, and enhance the traceability of reagent use. It makes the in-department reagent management more standardized, improves the reagent use efficiency, avoids waste and controls the cost. And through the high-quality information management of the reagent batch quality control, it better ensures the requirements in aspects such as reagent repeatability, sensitivity, and specificity, making the pathological diagnosis results accurate and reliable. BRIEF DESCRIPTION OF THE DRAWINGS

[0031] Figure 1 It is a flowchart of a quality control information management method for a pathological reagent provided by an exemplary embodiment of the present disclosure;

[0032] Figure 2 It is a schematic diagram of an application scenario of a quality control information management method for a pathological reagent provided by an exemplary embodiment of the present disclosure;

[0033] Figure 3 It is a schematic diagram of an interaction interface of a quality control information management method for a pathological reagent provided by an exemplary embodiment of the present disclosure;

[0034] Figure 4 It is a schematic diagram of modules of a quality control information management system for a pathological reagent provided by an exemplary embodiment of the present disclosure;

[0035] Figure 5 It is a schematic diagram of the structure of an electronic device provided by an exemplary embodiment of the present disclosure. DETAILED DESCRIPTION OF THE EMBODIMENTS

[0036] The present disclosure will be further described below by way of examples, but the present disclosure is not limited to the scope of the described examples.

[0037] In the embodiments of the present disclosure, prefix words such as "first" and "second" are only used to distinguish different described objects, and have no restrictive effect on the position, order, priority, quantity, content, etc. of the described objects. The use of prefix words such as ordinal numbers for distinguishing described objects in the embodiments of the present disclosure does not constitute a restriction on the described objects. For the statements of the described objects, refer to the descriptions in the context of the embodiments, and no redundant restrictions should be formed due to the use of such prefix words. In addition, in the description of this embodiment, unless otherwise specified, the meaning of "a plurality" is two or more.

[0038] Figure 1 It is a flowchart for quality control between batches of reagents in the prior art, mainly relying on manual registration of reagent incoming and outgoing. This method has a long execution process, requires a large number of paper record forms and label information to be filled in manually, is time-consuming and laborious, has low efficiency, and is difficult to execute. Moreover, the training cycle of professional pathological technicians is long, and the quality experiments between batches mainly rely on experienced pathological technicians. However, even very experienced technicians cannot guarantee complete error-free, and there are also problems with differences in filling habits among different personnel.

[0039] There are a wide variety of reagents. Taking reagents containing antibodies as an example, there are about 285 varieties of effective antibodies detected in the department. Almost every day, different reagents arrive. The process of batch comparison includes steps such as new reagent warehousing, printing comparison forms and slides, experimental operations, result reading and archiving, etc., which are time-consuming and laborious, and the work efficiency of personnel is low.

[0040] Based on this, the embodiments of the present disclosure provide a method for managing quality control information of pathological reagents, which can manage the quality control information of pathological reagents online, make the management of reagents in the department more standardized, improve the reagent use efficiency, avoid waste, control costs, and improve benefits. And through the high-quality informatization management of batch quality control of immunohistochemical antibodies, it can better ensure the requirements for repeatability, sensitivity, specificity, etc. of immunohistochemical antibodies, making the pathological diagnosis results accurate and reliable.

[0041] See Figure 1 and Figure 2 , the quality control information management method includes the following steps:

[0042] Step 101, obtain the reagent information recorded in the first reagent label of the incoming and outgoing reagents.

[0043] The quality control experiment between batches can be carried out for newly warehoused reagents. Newly warehoused reagents such as pathological reagents. The reagent information of newly warehoused reagents is generally provided by the reagent manufacturer and includes production information. The reagent information of newly warehoused reagents can but is not limited to include at least one of the following parameters: manufacturer identification, item number, reagent name, expiration date, production time, original batch number (old batch number), etc.

[0044] Batch - level quality control experiments can be carried out on the reagents to be shipped out. For example, a secondary batch - level quality control experiment can be carried out on the reagents to be shipped out. The reagent information of the reagents to be shipped out includes all or part of the quality control information of the previous batch - level quality control experiment and / or all or part of the reagent information provided by the manufacturer. The reagent information of the reagents to be shipped out can include, but is not limited to, at least one of the following parameters: manufacturer identification, product number, reagent name, batch number, expiration date, storage time, storage location number, batch number of the previous batch - level quality control experiment, experimental date of the previous batch - level quality control experiment, etc.

[0045] In one embodiment, the first reagent label is implemented by a barcode. By using a barcode scanner or triggering a mini - program to scan the barcode, the reagent information recorded in the first reagent label can be obtained.

[0046] The barcode can include, but is not limited to, barcodes, two - dimensional codes, etc. The barcode can be provided on the carrier component of the reagent or laser - printed on the carrier component of the reagent. The carrier component of the reagent can include, but is not limited to, glass slides, cover plates, reagent bottles, etc.

[0047] Figure 3 A schematic diagram of an interaction interface provided for an exemplary embodiment of the present disclosure. The obtained reagent information can be displayed through this interaction interface. The pathological technicians can verify the content displayed on the interaction interface. If there are problems during verification, corrections can be made. The interaction interface can be a WEB interface or an application program interface. The specific implementation method is not particularly limited in the embodiments of the present disclosure.

[0048] It should be noted that the reagent information can be all the information included in the scan result or some key information included in the scan result. Which information parameters of the scan result the reagent information specifically includes can be configured according to actual needs.

[0049] In one embodiment, some key information (target parameters) included in the scan result is extracted through an information entry template. Specifically, the barcode is scanned to obtain the initial information, and the second information entry template is used to extract the target parameters included in the initial information to obtain the reagent information including the target parameters; among them, the storage template includes fields corresponding to the target parameters.

[0050] For example, the first information entry template includes the following fields: manufacturer identification, product number, reagent name, expiration date, production time, original batch number. The field values corresponding to the manufacturer identification, product number, reagent name, expiration date, production time, and original batch number are respectively extracted from the initial information to obtain the reagent information.

[0051] Step 102: Obtain the quality control information obtained from the batch - level quality control experiment on the reagent.

[0052] Taking the reagent as an antibody as an example, when conducting an inter-batch quality control experiment on the antibody, at least 1 positive and 1 negative control should be used for traceability. After the batch of slides is sliced, staining is completed successively according to the staining procedure verified by the department. Through the inter-batch quality control experiment, the situation of using unqualified batch antibodies to detect clinical samples can be effectively prevented, the performance stability between different batches of reagents can be ensured, the experimental quality, the accuracy and repeatability of the experimental results can be improved. The specific implementation process of the inter-batch quality control experiment can be found in the relevant technical description and will not be elaborated here.

[0053] The quality control information can include, but is not limited to, at least one of the following parameters: the name of the reagent in the inter-batch quality control experiment, the original batch number, the new batch number (new batch ID), the experimental date, the information of the pathological technician, the experimental result, the impact on the clinical diagnosis result, etc. The new batch number can be provided by the pathological technician who conducts the inter-batch quality control experiment, and the writing rules of the new batch number can be unified for convenient information management.

[0054] Some of the parameters included in the quality control information are the same as some of the parameters included in the reagent information to achieve the binding of the subsequent quality control information and reagent information.

[0055] In one embodiment, the quality control information is obtained through an interactive interface. Specifically, in response to the quality control information input instruction, a first information input template matching the quality control information input instruction is displayed, the quality control data filled in the first information input template is obtained, and the quality control information is generated according to the first information input template.

[0056] The first information input template can be displayed through Figure 3 the interactive interface shown. If the first information input template is displayed through Figure 3 the interactive interface shown, in addition to the controls shown in the figure, controls for filling in quality control data such as the new batch number (new batch ID), the experimental date, the information of the pathological technician, the experimental result, etc. should also be displayed. After the pathological technician fills in the quality control data in the first information input template, the quality control information can be generated according to the data in the first information input template. In addition to Figure 3 all or part of the data currently displayed, the quality control information also includes all or part of the quality control data filled in by the pathological technician. Which parameters the quality control information specifically includes can be configured according to actual needs.

[0057] Step 103: Generate a second reagent label recording all or part of the reagent information and quality control information.

[0058] Among them, the second reagent label is a newly received and warehoused label. When the warehousing entity is a department, the second reagent label is a newly received and warehoused label of the department. The newly received and warehoused label can be a newly received label after procurement or a newly warehoused label after quality control experiments between n batches, where n is an integer greater than or equal to 1. The reagent information of the reagent and the quality control information of each batch of quality control experiments in the department can be obtained through the second reagent label.

[0059] The second reagent label can contain all the obtained reagent information and quality control information, or all the reagent information and part of the quality control information, or part of the reagent information and all the quality control information, or part of the reagent information and part of the quality control information. Which information parameters the second reagent label specifically contains can be configured according to actual needs.

[0060] In this embodiment, a new reagent label (the second reagent label) can be automatically generated to realize the standardized management of the quality control information of the reagent, reduce the manual copying link, improve work efficiency and the accuracy of records, realize record standardization, and enhance the traceability of reagent use. It makes the reagent management within the department more standardized, improves the reagent use efficiency, avoids waste and controls costs. And through the high-quality information management of reagent batch quality control, it better ensures the requirements in aspects such as reagent repeatability, sensitivity, and specificity, making the pathological diagnosis results accurate and reliable.

[0061] In one embodiment, after step 103, it further includes: sending the second reagent label to a printer for printing. The printed second reagent label can be affixed to the carrier component of the reagent. The carrier component of the reagent can include, but is not limited to, glass slides, cover plates, reagent bottles, etc.

[0062] It can be understood that the user can select the second reagent label of the reagent to be printed by themselves.

[0063] In one embodiment, the second reagent label is represented by a barcode, which can be a two-dimensional code or a barcode. The specific implementation method is not particularly limited in the embodiments of the present disclosure.

[0064] In this embodiment, the printer can include, but is not limited to, a fully automatic glass slide numbering machine (including two types of laser inkjet glass slides) or a common inkjet printer. Through a two-way communication connection, data exchange is realized between the printer and the system corresponding to the reagent quality control information management method of the embodiments of the present disclosure, so as to automatically print the second reagent label without manually inputting detection information such as pathological numbers and reagent information.

[0065] Specifically, this system can implement complex data processing and automated tasks through VBA (a development language) and Python (a development language), and then realize the quality control information management of reagents. This system can synchronously send the pre-set data to the printer to achieve batch quality control informatization management and printing of reagents.

[0066] In one embodiment, both the reagent information and the quality control information include the batch number of the reagent; the quality control information management method further includes: associatively storing the reagent information and the quality control information in a database according to the batch number. Associative storage means binding the reagent information and the quality control information, so as to realize the historical traceability of the data of the quality control experiment between batches. The associatively stored data are reagents purchased at different times and entering the department / laboratory at different times. Even if the batch numbers are the same, inter-batch quality control is required. After passing the quality control, they are used for clinical testing.

[0067] In this embodiment, it can automatically realize the associative storage of reagent information and quality control information, reduce the manual copying link, and avoid errors. Moreover, the warehoused data can realize effective information sharing, electronically manage reagents, so that the reagent information and quality control information can be retrieved at any time.

[0068] In one embodiment, the quality control information management method further includes: in response to a comparison instruction for a target batch, extracting from the database the quality control information obtained from the inter-batch quality control experiment that matches the target batch to compare the quality control results. Comparing the quality control results includes the comparison results of the quality control information of reagents purchased at different times and entering the department / laboratory at different times.

[0069] The quality control results can include, but are not limited to: information such as the differences between different batches of the same antibody produced by the same manufacturer and whether the differences meet the standards. In the case where it is determined that the differences do not meet the standards, an alarm message can be generated to prompt the pathological technicians. The above standards can be set according to the reagent situation.

[0070] In this embodiment, it is possible to record the quality system of the entire life cycle of the reagent, evaluate the quality control elements and quality control results of the reagent, compare the quality control results monthly and annually, and also track whether the differences between different batches of the same antibody produced by the same manufacturer will affect the clinical diagnosis results.

[0071] In one embodiment, the quality control information extracted from the database is displayed in the form of a table. In response to a print instruction, the table can also be printed. Specifically, the quality control information is transcribed into a table according to the set quality control template.

[0072] In one embodiment, the quality control results after comparing the reagents with the same batch number but different warehousing times are displayed in the form of a table. In response to a print instruction, the table can also be printed. Specifically, the quality control results are transcribed into a table according to the set quality control template.

[0073] In the past, record forms were all handwritten. In this embodiment, after the reagent information and quality control information are entered into the reagent management system, the system automatically extracts the old and new batch numbers of each reagent and transcribes and generates a form according to a set template for the convenience of the pathology technician to view.

[0074] Corresponding to the embodiment of the quality control information management method for the foregoing reagent, the present disclosure also provides an embodiment of a quality control information management system for the reagent.

[0075] Figure 4 It is a module schematic diagram of a quality control information management system for a reagent provided by an exemplary embodiment of the present disclosure. The system is used to implement the quality control information management method for the reagent provided in any of the foregoing embodiments. The system includes:

[0076] A first acquisition module 41, configured to acquire the reagent information recorded in the first reagent label of the incoming and outgoing reagent.

[0077] A second acquisition module 42, configured to acquire the quality control information obtained from the between-batch quality control experiment on the reagent.

[0078] A generation module 43, configured to generate a second reagent label recording all or part of the reagent information and the quality control information; the second reagent label is a newly received incoming label.

[0079] Optionally, the second acquisition module 42:

[0080] A display unit, in response to a quality control information entry instruction, displays a first information entry template matching the quality control information entry instruction.

[0081] An acquisition unit, acquires the quality control data filled in the first information entry template, and generates the quality control information according to the first information entry template.

[0082] Optionally, the first reagent label is a barcode provided on the carrier assembly of the reagent; the first acquisition module 41 is specifically configured to:

[0083] Scan the barcode to obtain initial information, and extract the target parameters included in the initial information by using a second information entry template to obtain reagent information including the target parameters; wherein, the incoming template includes fields corresponding to the target parameters.

[0084] Optionally, the reagent information and the quality control information include the batch number of the reagent; the quality control information management system further includes:

[0085] A storage module, configured to associate and store the reagent information and the quality control information in a database according to the batch number.

[0086] Optionally, it further includes:

[0087] A comparison module, configured to, in response to a comparison instruction of a target batch, extract quality control information obtained from an inter-batch quality control experiment that matches the target batch from the database, so as to compare the quality control results.

[0088] Optionally, it further includes:

[0089] A printing module, configured to send the second reagent label to a printer for printing;

[0090] And / or, the printing module is further configured to transcribe the quality control information into a table according to a set quality control template and print it.

[0091] For the system embodiment, since it basically corresponds to the method embodiment, the relevant parts can refer to the partial description of the method embodiment. The system embodiment described above is only illustrative, where the units described as separate components may or may not be physically separated, and the components as units may or may not be physical units, that is, they may be located in one place, or may be distributed to multiple network units. Some or all of the modules can be selected according to actual needs to achieve the purpose of the solution of the present disclosure.

[0092] Figure 5 It is a schematic structural diagram of an electronic device shown in an exemplary embodiment of the present disclosure. The electronic device includes a memory, a processor, and a computer program stored on the memory and configured to run on the processor. When the processor executes the computer program, it implements the method for managing quality control information of reagents described in any of the above embodiments. Figure 5 The electronic device 50 shown is only an example and should not bring any limitations to the functions and usage scope of the embodiments of the present disclosure.

[0093] As Figure 5 shown, the electronic device 50 can be presented in the form of a general computing device. For example, it can be a server device. The components of the electronic device 50 may include, but are not limited to: at least one of the above processors 51, at least one of the above memories 52, and a bus 53 connecting different system components (including the memory 52 and the processor 51).

[0094] The bus 53 includes a data bus, an address bus, and a control bus.

[0095] The memory 52 may include volatile memory, such as a random access memory (RAM) 521 and / or a cache memory 522, and may further include a read-only memory (ROM) 523.

[0096] The memory 52 may also include a program tool 525 (or utility) having a set (at least one) of program modules 524. Such program modules 524 include, but are not limited to: an operating system, one or more application programs, other program modules, and program data. Each of these examples or a certain combination thereof may include the implementation of a network environment.

[0097] The processor 51 executes various functional applications and data processing by running computer programs stored in the memory 52, such as the reagent quality control information management method provided in any of the above embodiments.

[0098] The electronic device 50 may also communicate with one or more external devices 54 (such as a keyboard, a pointing device, etc.). Such communication may be performed through the input / output (I / O) interface 55. And, the electronic device 50 may also communicate with one or more networks (such as a local area network (LAN), a wide area network (WAN), and / or a public network, such as the Internet) through the network adapter 56. As shown in the figure, the network adapter 56 communicates with other modules of the electronic device 50 through the bus 53. It should be understood that although not shown in the figure, other hardware and / or software modules may be used in combination with the electronic device 50, including but not limited to: microcode, device drivers, redundant processors, external disk drive arrays, RAID (redundant array of independent disks) systems, tape drives, and data backup storage systems, etc.

[0099] It should be noted that although several units / modules or sub-units / modules of the electronic device are mentioned in the above detailed description, this division is merely exemplary and not mandatory. In fact, according to the embodiments of the present disclosure, the features and functions of two or more of the above-described units / modules may be embodied in one unit / modules. Conversely, the features and functions of one unit / modules described above may be further divided and embodied by multiple unit / modules.

[0100] The embodiments of the present disclosure also provide a computer-readable storage medium, on which a computer program is stored. When the program is executed by a processor, it implements the reagent quality control information management method provided in any of the above embodiments.

[0101] Among them, the more specific readable storage medium that can be adopted may include, but is not limited to: a portable disk, a hard disk, a random access memory, a read-only memory, an erasable programmable read-only memory, an optical storage device, a magnetic storage device, or any suitable combination of the above.

[0102] The embodiments of the present disclosure also provide a computer program product, including a computer program. When the computer program is executed by a processor, it implements the reagent quality control information management method described in any of the above.

[0103] Among them, the program code for executing the computer program product of the present disclosure can be written in any combination of one or more programming languages, and the program code can be executed entirely on the user device, partially on the user device, executed as an independent software package, partially on the user device and partially on a remote device, or entirely on a remote device.

[0104] Although the specific embodiments of the present disclosure have been described above, those skilled in the art should understand that this is only an example, and the protection scope of the present disclosure is defined by the appended claims. Without departing from the principles and essence of the present disclosure, those skilled in the art can make various changes or modifications to these embodiments, but these changes and modifications all fall within the protection scope of the present disclosure.

Claims

1. A method for quality control information management of pathological reagents, characterized in that: include: Obtaining reagent information recorded in the first reagent label of the reagent entering or leaving the warehouse; Obtaining quality control information obtained from batch-to-batch quality control experiments on the reagent; A second reagent label recording all or part of the reagent information and the quality control information is generated; the second reagent label is a new label for receiving storage.

2. The quality control information management method for pathological reagents according to claim 1, characterized in that: Obtaining quality control information obtained by performing batch-to-batch quality control on the reagent, including: In response to a quality control information entry instruction, displaying a first information entry template matching the quality control information entry instruction; The quality control data filled in the first information entry template is obtained, and the quality control information is generated according to the first information entry template.

3. The quality control information management method for pathological reagents according to claim 1, characterized in that: The first reagent label is a barcode provided on the reagent carrier component; obtaining the reagent information recorded in the first reagent label of the reagent entering and leaving the warehouse includes: Scan the barcode to obtain initial information, and use the second information entry template to extract the target parameters contained in the initial information to obtain reagent information containing the target parameters; wherein the second information entry template contains a field corresponding to the target parameters.

4. The quality control information management method for pathological reagents according to claim 3, characterized in that: The reagent information and the quality control information both include the batch number of the reagent; the quality control information management method further includes: According to the batch number, the reagent information and the quality control information are associated and stored in a database.

5. The quality control information management method for pathological reagents according to claim 4, characterized in that: Also includes: In response to the comparison instruction of the target batch, quality control information obtained from the inter-batch quality control experiment matching the target batch is extracted from the database to compare the quality control results.

6. The method for quality control information management of pathological reagents according to any one of claims 1 to 5, characterized in that: Also includes: sending the second reagent label to a printer for printing; And / or, the quality control information is transcribed into a table and printed according to a set quality control template.

7. A quality control information management system for pathological reagents, characterized in that: include: A first acquisition module is used to acquire reagent information recorded in a first reagent label of a reagent entering or leaving the warehouse; A second acquisition module is used to obtain quality control information obtained by performing batch-to-batch quality control experiments on the reagent; A generating module is used to generate a second reagent label recording all or part of the reagent information and the quality control information; the second reagent label is a new label for receiving storage.

8. An electronic device comprising a memory, a processor, and a computer program stored in the memory and used to run on the processor, characterized in that: When the processor executes the computer program, the quality control information management method for a pathological reagent according to any one of claims 1 to 6 is implemented.

9. A computer-readable storage medium having a computer program stored thereon, characterized in that: When the computer program is executed by a processor, the method for managing quality control information of a pathological reagent according to any one of claims 1 to 6 is implemented.

10. A computer program product, comprising a computer program, characterized in that When the computer program is executed by a processor, the quality control information management method for a pathological reagent according to any one of claims 1 to 6 is implemented.

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