CN112951444A - Document processing method and system - Google Patents
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Abstract
The invention is suitable for the technical field of medical data processing, and provides a document processing method and a system, wherein the method comprises the following steps: acquiring a document to be processed; analyzing the document to be processed according to the document template corresponding to the document to be processed to obtain at least one field data; and mapping the field data according to the document template and the document to be processed to obtain a first structured data body. According to the invention, a clinical checker directly uploads a perfect file to be processed to a clinical experiment management system for document analysis, a structured data body obtained through analysis can be directly synchronized with a quality control platform, and the whole process is carried out on line, so that the process is effectively shortened, the dependence on fixed personnel is completely eliminated, the processing efficiency can be greatly improved, and the standardization of a clinical research file is facilitated.
Description
Technical Field
The invention belongs to the technical field of medical data processing, and particularly relates to a document processing method and a document processing system.
Background
Clinical studies refer to any systematic study of drugs in humans (either patients or healthy volunteers) to confirm or reveal the effects, adverse reactions, absorption, distribution, metabolism and excretion of the test drugs, with the purpose of determining the efficacy and safety of the test drugs.
The drug development process typically goes through 5 stages, including drug development initiatives, phase i clinical studies, phase ii clinical studies, phase iii clinical studies, and phase iv clinical studies. Wherein, the phase I clinical research refers to a careful test plan for researching the medicine in the human body for the first time, and the tested subjects are a small number of normal adult healthy volunteers and aim to observe the action mechanism of the medicine in the human body; phase ii clinical studies refer to studies performed on patients with established indications only, with the aim of finding the optimal dosage range and considering therapeutic feasibility; phase iii clinical studies refer to determining the effectiveness and safety, benefit and hazard ratio of study drugs; the phase IV clinical study refers to a large-scale study after the new drug is approved to be registered and marketed, and adverse reactions and toxicity during the general clinical use are examined.
During the clinical research, a large number of relevant documents such as quality control check reports, inspection reports, and audit reports are generated. At present, documents generated by clinical research are sequentially transferred and processed among responsible persons in relevant links in an off-line handover mode, and the processing efficiency is low.
Disclosure of Invention
In view of this, embodiments of the present invention provide a document processing method and apparatus, so as to solve the technical problem in the prior art that processing efficiency is low when processing a document generated by clinical research.
A first aspect of an embodiment of the present invention provides a document processing method, including:
acquiring a document to be processed;
analyzing the document to be processed according to the document template corresponding to the document to be processed to obtain at least one field data;
and mapping the field data according to the document template and the document to be processed to obtain a first structured data body.
A second aspect of an embodiment of the present invention provides a document processing system, including:
the first acquisition module is used for acquiring a document to be processed;
the analysis module is used for analyzing the document to be processed according to the document template corresponding to the document to be processed so as to obtain at least one field data;
and the mapping module is used for mapping the field data according to the document template and the document to be processed so as to obtain a first structured data body.
A third aspect of the embodiments of the present invention provides a terminal device, including a memory, a processor, and a computer program stored in the memory and executable on the processor, where the processor implements the document processing method described above when executing the computer program.
A fourth aspect of the embodiments of the present invention provides a computer-readable storage medium storing a computer program that, when executed by a processor, implements the document processing method described above.
Compared with the prior art, the embodiment of the invention has the following beneficial effects:
(1) according to the document processing method provided by the embodiment of the invention, by constructing the clinical experiment management system, a clinical checker directly uploads the perfect file to be processed (such as a checking report) to the clinical experiment management system for document analysis, the structured data body obtained through analysis can be directly synchronized with the quality control platform, and the whole process is carried out on line, so that the flow is effectively shortened, the dependence on fixed personnel is completely eliminated, and the processing efficiency can be greatly improved.
(2) When the embodiment of the invention acquires the document to be processed, the clinical checker can fill the content through the unified document template, which is beneficial to realizing the standardization of the clinical research document.
Drawings
In order to more clearly illustrate the technical solutions in the embodiments of the present invention, the drawings needed for the embodiments or the prior art descriptions will be briefly described below, and it is obvious that the drawings in the following description are only some embodiments of the present invention, and it is obvious for those skilled in the art to obtain other drawings without creative efforts.
FIG. 1 is a first flowchart illustrating a document processing method according to an embodiment of the present invention;
FIG. 2 is a flowchart illustrating a second implementation of a document processing method according to an embodiment of the present invention;
FIG. 3 is a flowchart of an implementation of obtaining field data in a document processing method according to an embodiment of the present invention;
FIG. 4 is a flowchart of an implementation of obtaining a first structured data volume in a document processing method according to an embodiment of the present invention;
FIG. 5 is a third schematic flow chart illustrating an implementation of a document processing method according to an embodiment of the present invention;
FIG. 6 is a flowchart illustrating a document processing method according to an embodiment of the present invention;
FIG. 7 is a first diagram of a document processing system provided by an embodiment of the invention;
FIG. 8 is a second schematic diagram of a document processing system provided by an embodiment of the present invention;
FIG. 9 is a diagram illustrating a parsing module in a document processing system, according to an embodiment of the invention;
fig. 10 is a schematic diagram of a terminal device according to an embodiment of the present invention.
Detailed Description
In the following description, for purposes of explanation and not limitation, specific details are set forth, such as particular system structures, techniques, etc. in order to provide a thorough understanding of the embodiments of the invention. It will be apparent, however, to one skilled in the art that the present invention may be practiced in other embodiments that depart from these specific details. In other instances, detailed descriptions of well-known systems, devices, circuits, and methods are omitted so as not to obscure the description of the present invention with unnecessary detail.
In order to explain the technical means of the present invention, the following description will be given by way of specific examples.
Referring to fig. 1, the present embodiment provides a document processing method, including:
step S11: and acquiring a document to be processed.
In the present embodiment, the type of the document to be processed can be set as needed. For example, the documents to be processed may be audit reports or audit reports obtained during a clinical study, etc. The report types are different, and the corresponding document templates are also different. Taking the inspection report as an example, a project clinical inspector writes and fills contents of corresponding parts of the document template corresponding to the inspection report according to the condition of a clinical research project, thereby obtaining the document to be processed. After the to-be-processed document is perfected, the project clinical inspector uploads the to-be-processed document to the clinical experiment management system, and the to-be-processed document can be further processed by the clinical experiment management system after the to-be-processed document is obtained. When the documents to be processed with the same name are repeatedly uploaded, the latest document to be processed uploaded serves as the standard.
The way for the project clinical inspector to acquire the document template can be selected according to actual needs.
In one embodiment, the project clinical inspector can directly obtain the document template offline through the line, for example, the project clinical inspector has already provided document templates for different clinical research projects according to past work experience, and when project research conditions need to be submitted, the project clinical inspector only needs to find the corresponding document template according to the clinical research projects, complete the corresponding part of the document template, and then upload the corresponding part to the clinical experiment management system, and the method is flexible.
In another embodiment, a project clinical inspector may download a corresponding document template via a clinical trial management system according to a clinical study project, and upload the corresponding document template to the clinical trial management system after completing a corresponding portion of the document template. Of course, when obtaining the document template in this way, the clinical experiment management system first needs to obtain the corresponding document template. Referring to fig. 2, at this time, step S11 further includes:
step S10: and acquiring a document template, and distributing an analysis identification code for the document template.
When the clinical experiment management system acquires the document template, a project clinical inspector uploads the document template to the clinical experiment management system through the clinical experiment management system background, the clinical experiment management system distributes corresponding analytic identification codes (analytic IDs) to different document templates and presets the analytic identification codes to the document templates, and different document templates correspond to different analytic identification codes, so that the document to be processed and the document template can be matched according to the analytic identification codes in the follow-up process, the matching speed is high, and the accuracy is high.
Of course, even if the document template is already stored in the clinical trial management system, the project clinical inspector can acquire the template in an off-line manner when acquiring the template, and does not need to download the template from the clinical trial management system every time when the project research situation needs to be perfected.
A document template is a template that can be structurally parsed, including attribute fields that vary from clinical trial item to clinical trial item. For example, the attribute fields of a document template may include: at least one of a mechanism acceptance number, a project name, a project state, a project phase, a project start time, and the like. The mechanism acceptance number and the project name are used as identification fields of the document template and can be used as identification conditions for subsequent document analysis. After the project clinical inspector obtains the document template, the contents of the corresponding parts are perfected according to the attribute fields in the document template, so that the document to be processed can be obtained.
Further, the frequency of acquiring the document to be processed by the clinical laboratory management system may be a fixed frequency, such as once a week, once a month, once a quarter, or once a half year, or may be a non-fixed frequency, and the clinical laboratory supervisor uploads the inspection report to the clinical laboratory management system after generating the inspection report or acquiring the inspection report/inspection report. When the clinical experiment management system acquires the document to be processed according to the fixed frequency, the clinical experiment management system may send a reminding message to a relevant person (e.g., a clinical inspector) according to the setting, so as to prompt the relevant person to upload the document to be processed, and the like. The sending mode of the reminding information may be sending through a mailbox, sending through a WeChat, sending through a short message, and the like, and the sending mode is not limited here.
Further, after the clinical experiment management system obtains the document to be processed, the document to be processed can be further analyzed and processed.
Step S12: and analyzing the document to be processed according to the document template corresponding to the document to be processed to obtain at least one field data.
In this embodiment, after acquiring the document to be processed, the clinical experiment management system may acquire a document template of the document to be processed, and parse the document to be processed according to a template structure of the document template. Referring to fig. 3, the process may include the following steps:
step S121: and acquiring a corresponding document template according to the analysis identification code of the document to be processed.
The document template is preset with an analysis ID, and the document to be processed obtained after the clinical inspector writes and fills the content of the document template still contains the analysis ID, so that the clinical experiment management system can obtain the corresponding document template according to the analysis ID after obtaining the document to be processed, and further can obtain the template structure of the document template.
Step S122: and analyzing the document to be processed according to the template structure of the document template so as to obtain field data corresponding to the attribute field in the template structure.
After the template structure of the document template is obtained, the file to be processed can be analyzed according to the template structure. For example, the template structure of a document template includes attribute fields such as a mechanism acceptance number, a project name, a project state, a project stage, and a project start time, and at this time, the attribute fields in the file to be processed can be correspondingly analyzed according to the template structure, and the corresponding content in each attribute field is analyzed, so as to obtain field data corresponding to the attribute fields, where the number of the field data is adapted to the number of the attribute fields.
It is understood that during the parsing process, the document parsing may also fail according to the actual situation of the uploaded document to be processed. For example, if the document to be processed uploaded to the clinical laboratory management system by the clinical inspector does not contain the preset parsing ID, the corresponding document template cannot be obtained from the clinical laboratory management system, and thus the document to be processed fails to be parsed. For another example, if the clinical inspector edits the attribute field again in the process of perfecting the corresponding attribute field according to the document template, so that the obtained overall structure of the document to be processed is different from that of the document template, or the attribute field is changed, the clinical experiment management system cannot analyze the attribute field in the analyzing process, and further cannot obtain corresponding field data, resulting in failure in analyzing the document to be processed. When the analysis of the file to be processed fails, the file to be processed which fails in the analysis is skipped over, and the next file to be processed is analyzed continuously. Of course, a prompt indicating that the analysis fails may also be returned, so that a clinical inspector may know the analysis result of the file to be processed, thereby prompting the clinical inspector to process the file to be processed that the analysis fails.
For the document to be processed that is successfully parsed, the field data obtained by parsing needs to be further processed.
Step S13: and mapping the field data according to the document template and the document to be processed to obtain a first structured data body.
The structured data body is structured data constructed according to a clinical research project, wherein the structured data body comprises information of various aspects of the clinical research project, the information is stored and correlated in a structured form, basic information, progress and the like of the clinical research project can be reflected, and contents in a document to be processed need to be correspondingly mapped to corresponding parts of the structured data body. For example, the attribute field in the document to be processed includes a mechanism acceptance number, an item name, an item state, an item stage, an item start time, and the like, and the structured data body also correspondingly includes a mechanism acceptance number, an item name, an item state, an item stage, an item start time, and the like, so that the field data of the attribute field in the document to be processed can be correspondingly mapped to the corresponding part of the structured data body. In this embodiment, the structured data body is a tree structure, a perfect fault tolerance mechanism is established, and the content of the document to be processed can be mapped to the tree structure in a machine learning manner, so that the structured tree data body can be obtained.
Referring to fig. 4, the process of mapping field data may be as follows:
step S131: and acquiring a corresponding second structured data body according to the identification field of the document to be processed.
Since the clinical laboratory management system stores structured data volumes of a plurality of clinical research projects, when mapping field data, it is necessary to obtain a mapping object of the field data of a document to be processed. In this embodiment, the identification field of the document to be processed includes an institution acceptance number and a project name, and the clinical laboratory management system can obtain the structured data body of the clinical research project stored therein according to the institution acceptance number and the project name, and mark the structured data body as the second structured data body. The second structured data volume stores all data from the clinical research project to date and is updated by periodic or aperiodic content fill.
Step S132: and correspondingly mapping the field data into the second structured data body according to the template structure of the document template to obtain a first structured data body.
After the second structured data volume is obtained, the clinical experiment management system may map the field data of different attribute fields into the second structured data volume according to the template structure of the document template, so as to obtain an updated second structured data volume, which is the first structured data volume. And meanwhile, after the mapping of the field data is finished, the document to be processed which is analyzed normally is stored.
After the document to be processed is processed, the field data of each attribute field in the document to be processed can be mapped to the structured data body, so that the data processing of the document to be processed is realized.
After the first structured data volume is obtained, quality control personnel are also required to perform quality control analysis on the clinical study. Referring to fig. 5, after step S13, the method further includes:
step S14: and synchronizing the structured data body with a quality control platform so as to perform quality control analysis on the structured data body.
In this embodiment, the clinical experiment management system synchronizes the updated structured data volume to the quality control platform, and the quality control personnel can acquire data of the clinical research project through the quality control platform, so that quality control analysis can be performed on the clinical research project. After the clinical experiment management system synchronizes the structured data body to the quality control platform, the clinical experiment management system can also send a reminding message to the quality control personnel to prompt the quality control personnel to perform quality control analysis in time, for example, the reminding message can be sent to the quality control personnel in a short message, WeChat or mail mode.
Referring to fig. 6, further, after the quality control analysis is completed, the clinical inspector can also check the result of the quality control analysis through the clinical experiment management system, and at this time, the clinical experiment management system can display the quality control analysis report on line.
Step S15: and displaying the first structured data body and/or the result of the quality control analysis on line.
The clinical experiment management system can display different types of data on line according to the request of a clinical inspector. For example, when a clinical inspector requests to view a first structured data volume, the clinical trial management system can provide an online viewing interface in which the updated first structured data volume is presented, such that the clinical inspector can visually understand the overall progress of the clinical study. For another example, when a clinical inspector requests to view a quality control analysis report, the quality control staff can send the quality control analysis report to a clinical experiment management system after completing the quality control analysis, and the clinical experiment management system can display the quality control analysis result on line according to the request of the clinical inspector.
The following describes a document processing method using a quality control audit report as an example.
The clinical inspector enters a quality control inspection report filling interface of the clinical experiment management system to acquire a document template, and the clinical experiment management system sends the document template to the clinical inspector (the document template can be directly downloaded or sent to a designated mailbox address). And after supplementing corresponding contents at the attribute field of the document template, the clinical inspector uploads the obtained document to be processed to the clinical experiment management system, the clinical experiment management system stores the structured data of the document to be processed in a warehouse to obtain an updated structured data body, and the updated structured data body is synchronized to the quality control platform. The quality control platform returns the synchronous result to the clinical experiment management system, and the clinical experiment management system returns the analysis result and the quality control analysis report to the clinical inspector, so that the clinical inspector can know the analysis condition of the document and the quality control analysis result of the clinical research project. When a quality control analysis report needs to be displayed on line, a clinical inspector can initiate a request to a quality control platform, and the quality control platform can display a quality control analysis result on line.
The document processing method provided by the embodiment has at least the following beneficial effects:
(1) currently, when performing document processing of clinical research projects, a complicated offline process is usually required: for quality control check reports and the like, a clinical checker sends the check reports to a clinical experiment coordinator in an off-line mode, the clinical experiment coordinator sends the completed check reports to a project manager/main researcher in an off-line mode, the project manager sends the check reports to a data analysis module for data analysis, a database file is exported, and the database data file is sent to a quality control platform in an off-line mode for quality control analysis. Not only the procedure is long, but also all processes are carried out in an off-line mode, so that the processing efficiency is low, and the processing is easy to forget and depends on fixed personnel to carry out.
According to the document processing method provided by the embodiment, by constructing the clinical experiment management system, a clinical checker directly uploads a perfect file to be processed (such as a check report) to the clinical experiment management system for document analysis, a structured data body obtained through analysis can be directly synchronized with the quality control platform, and the whole process is carried out on line, so that the flow is effectively shortened, the dependence on fixed personnel is completely eliminated, and the processing efficiency can be greatly improved.
(2) The document in the embodiment can be automatically circulated among the systems and the platforms, so that the barriers of the document between the systems and the platforms are avoided, and the system file is communicated.
(3) When the document to be processed is acquired, the clinical examiner can fill the content through the unified document template, which is helpful for realizing the standardization of the clinical research document.
(4) In the document processing method provided by this embodiment, the location where the clinical experiment management system exists may be set as needed, for example, the location may be built in a public cloud, a private cloud, or a hybrid cloud system, and the setting manner is flexible and various.
Referring to fig. 7, the present embodiment is further directed to a document processing system, which includes a first obtaining module 21, a parsing module 22, and a mapping module 23. The first obtaining module 21 is configured to obtain a document to be processed; the parsing module 22 is configured to parse the document to be processed according to the document template corresponding to the document to be processed, so as to obtain at least one field data; the mapping module 23 is configured to map the field data according to the document template and the document to be processed, so as to obtain a first structured data volume.
Further, referring to fig. 8, the document processing system further includes a second obtaining module 20, where the second obtaining module 20 is configured to obtain a document template and assign an analysis identifier to the document template.
Further, referring to fig. 9, the parsing module 22 includes a template obtaining unit 221 and a parsing unit 222. The template obtaining unit 221 is configured to obtain a corresponding document template according to the parsing identifier of the document to be processed; the parsing unit 222 is configured to parse the document to be processed according to the template structure of the document template to obtain field data corresponding to the attribute field in the template structure.
Further, the mapping module 23 is configured to obtain a corresponding second structured data volume according to the identification field of the to-be-processed document; and correspondingly mapping the field data into the second structured data body according to the template structure of the document template to obtain a first structured data body.
Further, the document processing system further includes a synchronization module 24, and the synchronization module 24 is configured to synchronize the structured data volume with the quality control platform, so as to perform quality control analysis on the structured data volume.
Further, the document processing system further comprises a display module 25, and the display module 25 is configured to display the first structured data volume and/or the result of the quality control analysis on line.
Fig. 10 is a schematic diagram of a terminal device according to an embodiment of the present invention. As shown in fig. 10, the terminal device 3 of this embodiment includes: a processor 30, a memory 31, and a computer program 32 stored in the memory 31 and executable on the processor 30. The steps in the various document processing method embodiments described above are implemented when the processor 30 executes the computer program 32.
Illustratively, the computer program 32 may be divided into one or more modules/units, which are stored in the memory 31 and executed by the processor 30 to carry out the invention. One or more of the modules/units may be a series of computer program instruction segments capable of performing specific functions, which are used to describe the execution of the computer program 32 in the terminal device 3.
The terminal device 3 may be a desktop computer, a notebook, a palm computer, a cloud server, or other computing devices. The terminal device 3 may include, but is not limited to, a processor 30, a memory 31. Those skilled in the art will appreciate that fig. 10 is merely an example of the terminal device 3, and does not constitute a limitation of the terminal device 3, and may include more or less components than those shown, or combine some of the components, or different components, for example, the terminal device 3 may further include an input-output device, a network access device, a bus, etc.
The Processor 30 may be a Central Processing Unit (CPU), other general purpose Processor, a Digital Signal Processor (DSP), an Application Specific Integrated Circuit (ASIC), a Field Programmable Gate Array (FPGA) or other Programmable logic device, discrete Gate or transistor logic, discrete hardware components, etc. A general purpose processor may be a microprocessor or the processor may be any conventional processor or the like.
The storage 31 may be an internal storage unit of the terminal device 3, such as a hard disk or a memory of the terminal device 3. The memory 31 may also be an external storage device of the terminal device 3, such as a plug-in hard disk provided on the terminal device 3, a Smart Media Card (SMC), a Secure Digital (SD) Card, a Flash memory Card (Flash Card), and the like. Further, the memory 31 may also include both an internal storage unit of the terminal device 3 and an external storage device. The memory 31 is used for storing computer programs and other programs and data required by the terminal device 3. The memory 31 may also be used to temporarily store data that has been output or is to be output.
It will be apparent to those skilled in the art that, for convenience and brevity of description, only the above-mentioned division of the functional units and modules is illustrated, and in practical applications, the above-mentioned function distribution may be performed by different functional units and modules according to needs, that is, the internal structure of the apparatus is divided into different functional units or modules, so as to perform all or part of the functions described above. Each functional unit and module in the embodiments may be integrated in one processing unit, or each unit may exist alone physically, or two or more units are integrated in one unit, and the integrated unit may be implemented in a form of hardware, or in a form of software functional unit. In addition, specific names of the functional units and modules are only for convenience of distinguishing from each other, and are not used for limiting the protection scope of the present application. The specific working processes of the units and modules in the system may refer to the corresponding processes in the foregoing method embodiments, and are not described herein again.
In the above embodiments, the descriptions of the respective embodiments have respective emphasis, and reference may be made to the related descriptions of other embodiments for parts that are not described or illustrated in a certain embodiment.
Those of ordinary skill in the art will appreciate that the various illustrative elements and algorithm steps described in connection with the embodiments disclosed herein may be implemented as electronic hardware or combinations of computer software and electronic hardware. Whether such functionality is implemented as hardware or software depends upon the particular application and design constraints imposed on the implementation. Skilled artisans may implement the described functionality in varying ways for each particular application, but such implementation decisions should not be interpreted as causing a departure from the scope of the present invention.
In the embodiments provided in the present invention, it should be understood that the disclosed apparatus/terminal device and method may be implemented in other ways. For example, the above-described embodiments of the apparatus/terminal device are merely illustrative, and for example, a module or a unit may be divided into only one logical function, and may be implemented in other ways, for example, a plurality of units or components may be combined or integrated into another system, or some features may be omitted or not executed. In addition, the shown or discussed mutual coupling or direct coupling or communication connection may be an indirect coupling or communication connection through some interfaces, devices or units, and may be in an electrical, mechanical or other form.
Units described as separate parts may or may not be physically separate, and parts displayed as units may or may not be physical units, may be located in one place, or may be distributed on a plurality of network units. Some or all of the units can be selected according to actual needs to achieve the purpose of the solution of the embodiment.
In addition, functional units in the embodiments of the present invention may be integrated into one processing unit, or each unit may exist alone physically, or two or more units are integrated into one unit. The integrated unit can be realized in a form of hardware, and can also be realized in a form of a software functional unit.
The integrated modules/units, if implemented in the form of software functional units and sold or used as separate products, may be stored in a computer readable storage medium. Based on such understanding, all or part of the flow in the method according to the embodiments of the present invention may also be implemented by a computer program, which may be stored in a computer-readable storage medium and used by a processor to implement the steps of the above-described embodiments of the method. Wherein the computer program comprises computer program code, which may be in the form of source code, object code, an executable file or some intermediate form, etc. The computer readable medium may include: any entity or device capable of carrying computer program code, recording medium, U.S. disk, removable hard disk, magnetic disk, optical disk, computer Memory, Read-Only Memory (ROM), Random Access Memory (RAM), electrical carrier wave signals, telecommunications signals, software distribution media, and the like. It should be noted that the computer readable medium may contain other components which may be suitably increased or decreased as required by legislation and patent practice in jurisdictions, for example, in some jurisdictions, in accordance with legislation and patent practice, the computer readable medium does not include electrical carrier signals and telecommunications signals.
The above-mentioned embodiments are only used for illustrating the technical solutions of the present invention, and not for limiting the same; although the present invention has been described in detail with reference to the foregoing embodiments, it will be understood by those of ordinary skill in the art that: the technical solutions described in the foregoing embodiments may still be modified, or some technical features may be equivalently replaced; such modifications and substitutions do not substantially depart from the spirit and scope of the embodiments of the present invention, and are intended to be included within the scope of the present invention.
Claims (10)
1. A method of document processing, comprising:
acquiring a document to be processed;
analyzing the document to be processed according to the document template corresponding to the document to be processed to obtain at least one field data;
and mapping the field data according to the document template and the document to be processed to obtain a first structured data body.
2. The document processing method of claim 1, wherein before the step of obtaining the document to be processed, further comprising:
and acquiring a document template, and distributing an analysis identification code for the document template.
3. The document processing method according to claim 1, wherein the parsing the document to be processed according to the document template corresponding to the document to be processed to obtain at least one field data comprises:
acquiring a corresponding document template according to the analysis identification code of the document to be processed;
and analyzing the document to be processed according to the template structure of the document template so as to obtain field data corresponding to the attribute field in the template structure.
4. The document processing method according to claim 1, wherein said mapping the field data according to the document template and the document to be processed to obtain a first structured data body comprises:
acquiring a corresponding second structured data body according to the identification field of the document to be processed;
and correspondingly mapping the field data into the second structured data body according to the template structure of the document template to obtain a first structured data body.
5. The document processing method of claim 1, wherein before the step of obtaining the document to be processed, further comprising:
and sending reminding information to related personnel to remind the related personnel to provide the document to be processed.
6. The document processing method according to any one of claims 1 to 5, wherein after the step of mapping the field data according to the template structure of the document template to obtain the structured data volume, the method further comprises:
and synchronizing the structured data body with a quality control platform so as to perform quality control analysis on the structured data body.
7. The document processing method of claim 6, wherein after the step of synchronizing the structured data volume with a quality control platform to perform quality control analysis on the structured data volume, further comprising:
and displaying the first structured data body and/or the result of the quality control analysis on line.
8. A document processing system, comprising:
the first acquisition module is used for acquiring a document to be processed;
the analysis module is used for analyzing the document to be processed according to the document template corresponding to the document to be processed so as to obtain at least one field data;
and the mapping module is used for mapping the field data according to the document template and the document to be processed so as to obtain a first structured data body.
9. A terminal device comprising a memory, a processor and a computer program stored in the memory and executable on the processor, wherein the processor implements the document processing method according to any one of claims 1 to 7 when executing the computer program.
10. A computer-readable storage medium, in which a computer program is stored, which, when being executed by a processor, implements a document processing method according to any one of claims 1 to 7.
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114140810A (en) * | 2022-01-30 | 2022-03-04 | 北京欧应信息技术有限公司 | Method, apparatus and medium for structured recognition of documents |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106649223A (en) * | 2016-12-23 | 2017-05-10 | 北京文因互联科技有限公司 | Financial report automatic generation method based on natural language processing |
| CN107832443A (en) * | 2017-11-20 | 2018-03-23 | 郑州云海信息技术有限公司 | A kind of processing method, device and the medium of JSON document data |
| CN108492172A (en) * | 2018-03-13 | 2018-09-04 | 四川享宇金信金融服务外包有限公司 | loan material packaging method and device |
| CN110415831A (en) * | 2019-07-18 | 2019-11-05 | 天宜(天津)信息科技有限公司 | A kind of medical treatment big data cloud service analysis platform |
-
2019
- 2019-12-11 CN CN201911263781.2A patent/CN112951444A/en active Pending
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106649223A (en) * | 2016-12-23 | 2017-05-10 | 北京文因互联科技有限公司 | Financial report automatic generation method based on natural language processing |
| CN107832443A (en) * | 2017-11-20 | 2018-03-23 | 郑州云海信息技术有限公司 | A kind of processing method, device and the medium of JSON document data |
| CN108492172A (en) * | 2018-03-13 | 2018-09-04 | 四川享宇金信金融服务外包有限公司 | loan material packaging method and device |
| CN110415831A (en) * | 2019-07-18 | 2019-11-05 | 天宜(天津)信息科技有限公司 | A kind of medical treatment big data cloud service analysis platform |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114140810A (en) * | 2022-01-30 | 2022-03-04 | 北京欧应信息技术有限公司 | Method, apparatus and medium for structured recognition of documents |
| CN114140810B (en) * | 2022-01-30 | 2022-04-22 | 北京欧应信息技术有限公司 | Method, apparatus and medium for structured recognition of documents |
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Application publication date: 20210611 |