CN113948164A - Clinical medicine management method, device, equipment and computer readable storage medium - Google Patents
Clinical medicine management method, device, equipment and computer readable storage medium Download PDFInfo
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H10/00—ICT specially adapted for the handling or processing of patient-related medical or healthcare data
- G16H10/20—ICT specially adapted for the handling or processing of patient-related medical or healthcare data for electronic clinical trials or questionnaires
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F16/00—Information retrieval; Database structures therefor; File system structures therefor
- G06F16/10—File systems; File servers
- G06F16/11—File system administration, e.g. details of archiving or snapshots
- G06F16/116—Details of conversion of file system types or formats
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F21/00—Security arrangements for protecting computers, components thereof, programs or data against unauthorised activity
- G06F21/60—Protecting data
- G06F21/602—Providing cryptographic facilities or services
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H70/00—ICT specially adapted for the handling or processing of medical references
- G16H70/40—ICT specially adapted for the handling or processing of medical references relating to drugs, e.g. their side effects or intended usage
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F2221/00—Indexing scheme relating to security arrangements for protecting computers, components thereof, programs or data against unauthorised activity
- G06F2221/21—Indexing scheme relating to G06F21/00 and subgroups addressing additional information or applications relating to security arrangements for protecting computers, components thereof, programs or data against unauthorised activity
- G06F2221/2107—File encryption
Abstract
The invention discloses a method, a device, equipment and a computer readable storage medium for managing clinical drugs, wherein the method comprises the following steps: when production information of a drug to be managed is received, acquiring clinical stage information of the drug to be managed, and generating a drug management file based on the clinical stage information; when an information change instruction is detected, acquiring a target file corresponding to the information change instruction in the medicine management file; and changing the target file according to the information changing instruction to obtain a first file, and generating a target identification code based on the first file. According to the invention, the medicine management file corresponding to the clinical stage is changed, the identification code is generated based on the changed medicine management file, and when the clinical information of the medicine in a certain clinical stage needs to be checked, only the identification code corresponding to the clinical stage needs to be scanned, so that the management cost of the clinical information of the medicine is reduced, and the convenience for checking the clinical information of the medicine is also improved.
Description
Technical Field
The present invention relates to the field of information management, and in particular, to a method, an apparatus, a device, and a computer-readable storage medium for clinical drug management.
Background
With the rapid development of scientific technology, the research and development speed of people on new drugs is improved, and the drugs are put into use, apart from the research and development process, clinical tests cannot be left, and are influenced by safety factors, most of the currently developed new drugs experience a long clinical test period, and the steps of the clinical test process are complicated.
Disclosure of Invention
The invention mainly aims to provide a clinical medicine management method, a clinical medicine management device, clinical medicine management equipment and a computer readable storage medium, and aims to solve the technical problems of high management cost and low convenience of the existing clinical medicine information.
In addition, in order to achieve the above object, the present invention further provides a clinical drug management method, including the steps of:
when production information of a drug to be managed is received, acquiring clinical stage information of the drug to be managed, and generating a drug management file based on the clinical stage information;
when an information change instruction is detected, acquiring a target file corresponding to the information change instruction in the medicine management file;
and changing the target file according to the information changing instruction to obtain a first file, and generating a target identification code based on the first file.
Optionally, the clinical stage information includes a target clinical stage, and the step of generating a drug management file based on the clinical stage information includes:
and generating a drug management file corresponding to the target clinical stage based on the file format and the target proportion corresponding to the target clinical stage.
Optionally, when an information change instruction is detected, the step of acquiring a target file corresponding to the information change instruction in the drug management file includes:
when an information change instruction is detected, acquiring a current clinical stage corresponding to the information change instruction, wherein the current clinical stage belongs to the target clinical stage;
and determining the drug management file corresponding to the current clinical stage based on the corresponding relation between the target clinical stage and the drug management file, and taking the drug management file corresponding to the current clinical stage as the target file corresponding to the information change instruction.
Optionally, the step of modifying the target file according to the information modification instruction to obtain a first file includes:
acquiring a format change rule, a proportion change rule and replacement information corresponding to the information change instruction;
and changing the file format and the target proportion of the target file based on the format change rule and the proportion change rule, and changing the clinical information contained in the target file based on the replacement information to obtain a first file.
Optionally, the step of generating the target identification code based on the first file includes:
if the first file is a local file, acquiring a local storage address of the first file and clinical information contained in the first file;
and generating a target identification code based on the local storage address and the encrypted information corresponding to the clinical information.
Optionally, the step of generating the target identification code based on the first file includes:
and if the first file is a network file, acquiring a network address of the first file, and generating a target identification code based on the network address.
Optionally, the first file is a local file, and after the step of generating the target identification code based on the first file, the method includes:
receiving a scanning instruction generated based on the target identification code, acquiring scanning equipment information corresponding to the scanning instruction, and judging whether the scanning equipment information is matched with the local storage address;
if the scanning equipment information is matched with the local storage address, outputting the clinical information through the local storage address;
and if the scanning equipment information does not match the local storage address, outputting the clinical information by verifying the encrypted information.
In order to achieve the above object, the present invention also provides a clinical medicine management apparatus including:
the system comprises a drug management file generation module, a drug management file generation module and a drug management file generation module, wherein the drug management file generation module is used for acquiring clinical stage information of a drug to be managed when production information of the drug to be managed is received, and generating a drug management file based on the clinical stage information;
the target file acquisition module is used for acquiring a target file corresponding to an information change instruction in the medicine management file when the information change instruction is detected;
and the target identification code generation module is used for changing the target file according to the information change instruction to obtain a first file and generating a target identification code based on the first file.
In addition, to achieve the above object, the present invention also provides a clinical medicine management apparatus including: a memory, a processor, and a clinical drug management program stored on the memory and executable on the processor, the clinical drug management program when executed by the processor implementing the steps of the clinical drug management method as described above.
In addition, to achieve the above object, the present invention also provides a computer readable storage medium having stored thereon a clinical drug management program, which when executed by a processor, implements the steps of the clinical drug management method as described above.
Furthermore, to achieve the above object, the present invention also provides a computer program product comprising a computer program which, when being executed by a processor, realizes the steps of the clinical medication management method as described above.
The embodiment of the invention provides a clinical medicine management method, a device, equipment and a computer readable storage medium. In the embodiment of the invention, when production information of a medicine to be managed is received, clinical stage information of the medicine to be managed is acquired, a medicine management file is generated based on the clinical stage information, when an information change instruction is detected, a target file corresponding to the information change instruction in the medicine management file is acquired, the target file is changed according to the information change instruction to obtain a first file, and finally a target identification code is generated based on the first file.
Drawings
FIG. 1 is a schematic diagram of a hardware configuration of an embodiment of a clinical medication management apparatus according to an embodiment of the present invention;
FIG. 2 is a schematic flow chart of a first embodiment of a method for clinical drug management according to the present invention;
FIG. 3 is a flowchart illustrating a second embodiment of a method for clinical drug management according to the present invention;
FIG. 4 is a functional block diagram of a clinical medication management apparatus according to an embodiment of the present invention.
The implementation, functional features and advantages of the objects of the present invention will be further explained with reference to the accompanying drawings.
Detailed Description
It should be understood that the specific embodiments described herein are merely illustrative of the invention and are not intended to limit the invention.
In the following description, suffixes such as "module", "component", or "unit" used to denote elements are used only for facilitating the explanation of the present invention, and have no specific meaning in itself. Thus, "module", "component" or "unit" may be used mixedly.
The clinical medicine management terminal (also called terminal, equipment or terminal equipment) in the embodiment of the invention can be a PC, or equipment with data processing function and identification code compiling function such as a smart phone, a tablet computer, a portable computer and the like, or equipment with identification code identification function.
As shown in fig. 1, the terminal may include: a processor 1001, such as a CPU (Central Processing Unit), a communication bus 1002, and a memory 1003. Wherein a communication bus 1002 is used to enable connective communication between these components. The memory 1003 may be a high-speed RAM memory or a non-volatile memory (e.g., a disk memory). The memory 1003 may alternatively be a storage device separate from the processor 1001.
Those skilled in the art will appreciate that the terminal structure shown in fig. 1 is not intended to be limiting and may include more or fewer components than those shown, or some components may be combined, or a different arrangement of components.
As shown in fig. 1, a clinical medication management program may be included in the memory 1003 as a kind of computer storage medium.
In the terminal shown in fig. 1, the processor 1001 may be configured to call the clinical drug management program stored in the memory 1003, and perform the following operations:
when production information of a drug to be managed is received, acquiring clinical stage information of the drug to be managed, and generating a drug management file based on the clinical stage information;
when an information change instruction is detected, acquiring a target file corresponding to the information change instruction in the medicine management file;
and changing the target file according to the information changing instruction to obtain a first file, and generating a target identification code based on the first file.
Further, the processor 1001 may be configured to call the clinical drug management program stored in the memory 1003, and further perform the following operations:
and generating a drug management file corresponding to the target clinical stage based on the file format and the target proportion corresponding to the target clinical stage.
Further, the processor 1001 may be configured to call the clinical drug management program stored in the memory 1003, and further perform the following operations:
when an information change instruction is detected, acquiring a current clinical stage corresponding to the information change instruction, wherein the current clinical stage belongs to the target clinical stage;
and determining the drug management file corresponding to the current clinical stage based on the corresponding relation between the target clinical stage and the drug management file, and taking the drug management file corresponding to the current clinical stage as the target file corresponding to the information change instruction.
Further, the processor 1001 may be configured to call the clinical drug management program stored in the memory 1003, and further perform the following operations:
acquiring a format change rule, a proportion change rule and replacement information corresponding to the information change instruction;
and changing the file format and the target proportion of the target file based on the format change rule and the proportion change rule, and changing the clinical information contained in the target file based on the replacement information to obtain a first file.
Further, the processor 1001 may be configured to call the clinical drug management program stored in the memory 1003, and further perform the following operations:
if the first file is a local file, acquiring a local storage address of the first file and clinical information contained in the first file;
and generating a target identification code based on the local storage address and the encrypted information corresponding to the clinical information.
Further, the processor 1001 may be configured to call the clinical drug management program stored in the memory 1003, and further perform the following operations:
and if the first file is a network file, acquiring a network address of the first file, and generating a target identification code based on the network address.
Further, the processor 1001 may be configured to call the clinical drug management program stored in the memory 1003, and further perform the following operations:
receiving a scanning instruction generated based on the target identification code, acquiring scanning equipment information corresponding to the scanning instruction, and judging whether the scanning equipment information is matched with the local storage address;
if the scanning equipment information is matched with the local storage address, outputting the clinical information through the local storage address;
and if the scanning equipment information does not match the local storage address, outputting the clinical information by verifying the encrypted information.
Based on the hardware structure of the equipment, the embodiment of the clinical medicine management method is provided.
It should be noted that the clinical phase of a new drug can be roughly divided into the phases of receiving a drug to be clinically tested, storing the drug to be clinically tested, dispensing the drug to an institution executing the clinical test, using the drug to be clinically tested, and recovering the drug after the clinical test, and each phase has corresponding data to be managed, for example, in the phase of receiving the drug to be clinically tested, the corresponding data can be the production information of the drug to be clinically tested, and preset clinical information (the number of clinical tests, the duration of the clinical tests, and the like).
Referring to fig. 2, in a first embodiment of the clinical drug management method of the present invention, the clinical drug management method includes:
step S10, when the production information of the drug to be managed is received, the clinical stage information of the drug to be managed is obtained, and a drug management file is generated based on the clinical stage information.
It should be noted that, in the present embodiment, the first phase of the default clinical medicine management is to receive production information of a medicine to be clinically tested (i.e., the medicine to be managed in the present embodiment), and then obtain clinical phase information preset for the medicine to be managed, where the clinical phase information includes information such as the number of clinical phases and duration corresponding to each clinical phase, and after obtaining the clinical phase information of the medicine to be managed, generate a medicine management file based on the clinical phase information, specifically, each clinical phase of the medicine to be managed has its corresponding management information generated, and these management information have fixed attributes, for example, when the medicine to be managed is in a use phase, its corresponding management information is time information and response information, and these information can be better stored in a form file; when the medicines to be managed are in the receiving stage, the corresponding management information is the medicine production information, and the information can be better stored in the document file. Therefore, the drug management file is generated based on the clinical stage information, and the number of files and the file attribute corresponding to each clinical stage, that is, the number and the attribute of the drug management file can be surely determined by each clinical stage in the clinical stage information.
Step S20, when an information change instruction is detected, a target file corresponding to the information change instruction in the drug management file is acquired.
After the drug management file is generated based on the clinical stage information, when the clinical stage changes, new information is generated without fail, and the generated new information is written into the drug management file. Specifically, if the clinical phase of the drug is changed from the receiving phase to the storing phase, the generated new information may be storage information (storage time, storage environment requirement, and the like) of the clinical drug, and the target file corresponding to the information change instruction is the drug management file corresponding to the storing phase, so that the target file in the embodiment belongs to the drug management file generated based on the clinical phase information.
And step S30, modifying the target file according to the information modification instruction to obtain a first file, and generating a target identification code based on the first file.
The method includes writing new information generated by clinical stage change into a target file based on an information change instruction, obtaining a first file after the writing is completed, namely the first file is the target file containing the new information generated by clinical stage change, and after the first file is obtained, encoding information contained in the first file through a preset encoding rule to generate a target identification code (for example, a two-dimensional code). It should be noted that the types and encoding manners of the first file are different, and specifically, when the first file is a file stored on a local server or a hard disk, the storage path of the file and information included in the file may be encoded, so that other devices may obtain the storage path of the first file after scanning the target identification code or directly output the information included in the first file; when the first file is a network file, the network address of the network file may be encoded, so that other devices may obtain the network address of the first file after scanning the target identification code, and then browse the network address to obtain information included in the first file.
Further, in a possible embodiment, the clinical stage information includes a target clinical stage, the step S10 is to generate a drug management file based on the clinical stage information, and the step of refining includes:
step S11, generating a drug management file corresponding to the target clinical stage based on the file format and the target ratio corresponding to the target clinical stage.
It should be noted that the clinical stage information is composed of each clinical stage and its corresponding file attribute, it can be understood that the clinical trial of the medicine includes a plurality of stages, and each stage has information that needs to be collected, the content and format of the information are fixed, for example, when the medicine to be managed is in the use stage, the corresponding management information is time information and response information, the information can be better stored in the form file, the format of the information here means that the representation form of the information in the file is represented in the form of table plus characters or directly in the form of characters, the target ratio in this embodiment means that each clinical stage corresponds to the number of files, the number of files corresponding to each clinical stage is the target ratio corresponding to this clinical stage, for example, the number of files corresponding to the receiving stage of the clinical medicine is 2, one file is used for recording the production information of the clinical medicines, and the other file is used for recording the storage conditions of the clinical medicines.
Further, in a possible embodiment, in the step S20, when an information change instruction is detected, the target file corresponding to the information change instruction in the drug management file is obtained, and the step of refining includes:
step S21, when an information change instruction is detected, acquiring a current clinical stage corresponding to the information change instruction, wherein the current clinical stage belongs to the target clinical stage;
step S22, determining the drug management file corresponding to the current clinical stage based on the correspondence between the target clinical stage and the drug management file, and using the drug management file corresponding to the current clinical stage as the target file corresponding to the information change instruction.
It should be noted that, when the clinical phase of the drug to be managed changes from one phase to another phase, an information change instruction is triggered to be generated, and the information change instruction is used to perform information filling (i.e. information change) on the drug management file corresponding to the phase to be changed (i.e. the current clinical phase in this embodiment), specifically, in the process of changing the clinical phase of the drug to be managed from the receiving phase to the storing phase, an information change instruction is triggered to be generated, and the current clinical phase corresponding to the information change instruction is the storing phase, the target clinical phase in this embodiment refers to all clinical phases of the drug to be managed, so the current clinical phase belongs to the target clinical phase, and each clinical phase of the drug to be managed has its corresponding drug management file (number and format), based on the corresponding relationship between the target clinical phase and the drug management file, the method includes the steps of determining a medicine management file corresponding to a current clinical stage, and then taking the medicine management file corresponding to the current clinical stage as a target file corresponding to an information change instruction, namely, a file needing information change, wherein the target file is changed to obtain a first file.
Further, in a possible embodiment, in step S30, the target file is modified according to the information modification instruction to obtain a first file, and the step of refining includes:
step S31, obtaining format change rule, proportion change rule and replacement information corresponding to the information change instruction;
step S32, based on the format modification rule and the scale modification rule, modifying the file format and the target scale of the target file, and based on the replacement information, modifying the clinical information included in the target file to obtain a first file.
It should be noted that, the format change rule, the ratio change rule and the replacement information corresponding to the information change instruction are preset and determined before the clinical stage of the drug to be managed changes, which is related to the current clinical stage corresponding to the information change instruction, the format and the target ratio of the drug management file (i.e. the target file in this embodiment) corresponding to the current clinical stage are determined in advance, and the clinical information that the target file needs to record is collected during the current clinical stage, first, the file format and the target ratio of the target file are changed based on the format change rule and the ratio change rule, then, the clinical information contained in the target file is changed based on the replacement information to obtain a first file, and as a matter of course, before the clinical information contained in the target file is changed based on the replacement information, the target file only comprises a basic frame for storing the replacement information, and the process of changing the clinical information contained in the target file based on the replacement information is to essentially fill the replacement information in the corresponding frame to obtain the first file.
Further, in a possible embodiment, in the step S30, the step of generating the target identifier based on the first document includes:
step S33, if the first file is a local file, acquiring a local storage address of the first file and clinical information included in the first file;
step S34, generating a target identification code based on the local storage address and the encrypted information corresponding to the clinical information.
It should be noted that the first file further includes multiple types, for example, a local file stored in a memory of the device, and if the first file is a local file, the local storage address of the first file and the clinical information of the drug contained in the first file are obtained, the local storage address of the first file and the encrypted information corresponding to the clinical information of the drug are encoded to generate the target identification code, it is known that the encrypted information corresponding to the clinical information of the drug refers to information obtained by encrypting the clinical information of the drug, when the clinical information of the drug relates to a privacy problem, the clinical information of the drug is encrypted, when a certain device scans the target identification code, the encrypted information needs to be verified first, the clinical information contained in the first file is output on the device after the verification is passed, and the first file serving as the local file can be quickly found through the local storage address, the clinical information contained in the first file is then output after the encrypted information is verified.
Further, in a possible embodiment, in the step S30, the step of generating the target identifier based on the first document further includes:
step S35, if the first file is a network file, acquiring a network address of the first file, and generating a target identification code based on the network address.
It should be noted that, in addition to the local file, the first file may also include other types, for example, a file stored in a network (for example, a cloud server), if the first file is a network file, a network address of the first file is obtained, then only the network address of the first file is encoded to obtain a target identification code, when a certain device scans the target identification code, the network address of the first file is obtained, and the drug clinical information included in the first file is checked by accessing the network address, specifically, after the device accesses the network address of the first file, verification of encrypted information may be further performed to protect the private information included in the first file.
In the embodiment, when production information of a medicine to be managed is received, clinical stage information of the medicine to be managed is acquired, a medicine management file is generated based on the clinical stage information, when an information change instruction is detected, a target file corresponding to the information change instruction in the medicine management file is acquired, the target file is changed according to the information change instruction to obtain a first file, and finally a target identification code is generated based on the first file.
Further, referring to fig. 3, a second embodiment of the clinical drug management method of the present invention is proposed on the basis of the above-mentioned embodiment of the present invention.
This embodiment is a step after step S30 in the first embodiment, and the present embodiment is different from the above-described embodiments of the present invention in that:
step S40, receiving a scanning instruction generated based on the target identification code, acquiring scanning device information corresponding to the scanning instruction, and determining whether the scanning device information matches the local storage address;
step S50, if the scanning device information matches the local storage address, outputting the clinical information via the local storage address;
step S60, if the scanning device information does not match the local storage address, outputting the clinical information by verifying the encrypted information.
It should be noted that, if the drug management file corresponding to each clinical stage is a local file, after the target identification code corresponding to each clinical stage is generated, when a scanning instruction generated based on the target identification code is received (scanning device), scanning device information corresponding to the scanning instruction is acquired, whether the scanning device information is matched with the local storage address is judged, wherein, the scanning device information is used for representing specific devices, and the judgment basis of whether the scanning device information is matched with the local storage address is that whether the medicine management file corresponding to the target identification code is stored on the scanning device corresponding to the scanning device information, if the medicine management file corresponding to the target identification code is stored on the scanning device corresponding to the scanning device information, determining that the scanning device information matches the local memory address, in which case the scanning device may directly access the local memory address and directly output the clinical information; if the medicine management file corresponding to the target identification code is not stored in the scanning device corresponding to the scanning device information, it is determined that the scanning device information is not matched with the local storage address, which proves that the medicine management file corresponding to the target identification code is not stored in the scanning device.
In the embodiment, the storage relationship between the scanning equipment and the medicine management file is judged by scanning the target identification code, whether the encrypted information needs to be verified or not is determined, and the safety of clinical information is ensured while the management cost of the clinical information of the medicine is reduced.
In addition, referring to fig. 4, an embodiment of the present invention further provides a clinical medicine management apparatus, including:
the drug management file generation module 10 is configured to, when production information of a drug to be managed is received, acquire clinical stage information of the drug to be managed, and generate a drug management file based on the clinical stage information;
the target file acquiring module 20 is configured to acquire a target file corresponding to an information change instruction in the drug management file when the information change instruction is detected;
and the target identification code generating module 30 is configured to modify the target file according to the information modification instruction to obtain a first file, and generate a target identification code based on the first file.
Optionally, the clinical stage information includes a target clinical stage, and the drug management file generating module 10 includes:
and the medicine management file generating unit is used for generating a medicine management file corresponding to the target clinical stage based on the file format and the target proportion corresponding to the target clinical stage.
Optionally, the target file obtaining module 20 includes:
the current clinical stage acquiring unit is used for acquiring a current clinical stage corresponding to an information change instruction when the information change instruction is detected, wherein the current clinical stage belongs to the target clinical stage;
and the determining unit is used for determining the medicine management file corresponding to the current clinical stage based on the corresponding relation between the target clinical stage and the medicine management file, and taking the medicine management file corresponding to the current clinical stage as the target file corresponding to the information change instruction.
Optionally, the target identification code generating module 30 includes:
the first obtaining unit is used for obtaining a format change rule, a proportion change rule and replacement information corresponding to the information change instruction;
and the information changing unit is used for changing the file format and the target proportion of the target file based on the format changing rule and the proportion changing rule, and changing the clinical information contained in the target file based on the replacing information to obtain a first file.
Optionally, the target identification code generating module 30 further includes:
the second obtaining unit is used for obtaining a local storage address of the first file and clinical information contained in the first file if the first file is a local file;
and the first target identification code generating unit is used for generating a target identification code based on the local storage address and the encrypted information corresponding to the clinical information.
Optionally, the target identification code generating module 30 further includes:
and the second target identification code generating unit is used for acquiring the network address of the first file if the first file is a network file, and generating a target identification code based on the network address.
Optionally, the first file is a local file, and the clinical drug management apparatus further includes:
the judging module is used for receiving a scanning instruction generated based on the target identification code, acquiring scanning equipment information corresponding to the scanning instruction, and judging whether the scanning equipment information is matched with the local storage address or not;
the first clinical information output module is used for outputting the clinical information through the local storage address if the scanning equipment information is matched with the local storage address;
and the second clinical information output module is used for outputting the clinical information by verifying the encrypted information if the scanning equipment information is not matched with the local storage address.
In addition, an embodiment of the present invention further provides a computer-readable storage medium, where a clinical drug management program is stored on the computer-readable storage medium, and when executed by a processor, the clinical drug management program implements operations in the clinical drug management method provided in the foregoing embodiment.
The method executed by each program module can refer to each embodiment of the method of the present invention, and is not described herein again.
It is noted that, herein, relational terms such as first and second, and the like may be used solely to distinguish one entity/action/object from another entity/action/object without necessarily requiring or implying any actual such relationship or order between such entities/actions/objects; the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or system that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or system. Without further limitation, an element defined by the phrase "comprising an … …" does not exclude the presence of other like elements in a process, method, article, or system that comprises the element.
For the apparatus embodiment, since it is substantially similar to the method embodiment, it is described relatively simply, and reference may be made to some descriptions of the method embodiment for relevant points. The above-described apparatus embodiments are merely illustrative, in that elements described as separate components may or may not be physically separate. Some or all of the modules can be selected according to actual needs to achieve the purpose of the scheme of the invention. One of ordinary skill in the art can understand and implement it without inventive effort.
The above-mentioned serial numbers of the embodiments of the present invention are merely for description and do not represent the merits of the embodiments.
Through the above description of the embodiments, those skilled in the art will clearly understand that the method of the above embodiments can be implemented by software plus a necessary general hardware platform, and certainly can also be implemented by hardware, but in many cases, the former is a better implementation manner. Based on such understanding, the technical solution of the present invention may be substantially or partially embodied in the form of a software product, which is stored in a storage medium (e.g., ROM/RAM, magnetic disk, optical disk) as described above and includes instructions for enabling a terminal device (e.g., a mobile phone, a computer, a server, an air conditioner, or a network device) to execute the method for clinical drug management according to the embodiments of the present invention.
The above description is only a preferred embodiment of the present invention, and not intended to limit the scope of the present invention, and all modifications of equivalent structures and equivalent processes, which are made by using the contents of the present specification and the accompanying drawings, or directly or indirectly applied to other related technical fields, are included in the scope of the present invention.
Claims (10)
1. A clinical drug management method, characterized in that the clinical drug management method comprises the following steps:
when production information of a drug to be managed is received, acquiring clinical stage information of the drug to be managed, and generating a drug management file based on the clinical stage information;
when an information change instruction is detected, acquiring a target file corresponding to the information change instruction in the medicine management file;
and changing the target file according to the information changing instruction to obtain a first file, and generating a target identification code based on the first file.
2. The clinical drug management method of claim 1, wherein the clinical stage information includes a target clinical stage, and the step of generating a drug management file based on the clinical stage information includes:
and generating a drug management file corresponding to the target clinical stage based on the file format and the target proportion corresponding to the target clinical stage.
3. The clinical drug management method according to claim 2, wherein the step of acquiring the target file corresponding to the information change instruction in the drug management file when the information change instruction is detected comprises:
when an information change instruction is detected, acquiring a current clinical stage corresponding to the information change instruction, wherein the current clinical stage belongs to the target clinical stage;
and determining the drug management file corresponding to the current clinical stage based on the corresponding relation between the target clinical stage and the drug management file, and taking the drug management file corresponding to the current clinical stage as the target file corresponding to the information change instruction.
4. The method for clinical drug management according to claim 3, wherein the step of modifying the target file according to the information modification instruction to obtain a first file comprises:
acquiring a format change rule, a proportion change rule and replacement information corresponding to the information change instruction;
and changing the file format and the target proportion of the target file based on the format change rule and the proportion change rule, and changing the clinical information contained in the target file based on the replacement information to obtain a first file.
5. The clinical drug management method of claim 1, wherein the step of generating a target identification code based on the first file comprises:
if the first file is a local file, acquiring a local storage address of the first file and clinical information contained in the first file;
and generating a target identification code based on the local storage address and the encrypted information corresponding to the clinical information.
6. The clinical drug management method of claim 1, wherein the step of generating a target identification code based on the first file comprises:
and if the first file is a network file, acquiring a network address of the first file, and generating a target identification code based on the network address.
7. The clinical drug management method of claim 5, wherein the first file is a local file, and wherein the step of generating the target identification code based on the first file is followed by:
receiving a scanning instruction generated based on the target identification code, acquiring scanning equipment information corresponding to the scanning instruction, and judging whether the scanning equipment information is matched with the local storage address;
if the scanning equipment information is matched with the local storage address, outputting the clinical information through the local storage address;
and if the scanning equipment information does not match the local storage address, outputting the clinical information by verifying the encrypted information.
8. A clinical drug management device, comprising:
the system comprises a drug management file generation module, a drug management file generation module and a drug management file generation module, wherein the drug management file generation module is used for acquiring clinical stage information of a drug to be managed when production information of the drug to be managed is received, and generating a drug management file based on the clinical stage information;
the target file acquisition module is used for acquiring a target file corresponding to an information change instruction in the medicine management file when the information change instruction is detected;
and the target identification code generation module is used for changing the target file according to the information change instruction to obtain a first file and generating a target identification code based on the first file.
9. A clinical drug management apparatus, characterized in that the clinical drug management apparatus comprises: a memory, a processor, and a clinical drug management program stored on the memory and executable on the processor, the clinical drug management program when executed by the processor implementing the steps of the clinical drug management method of any of claims 1 to 7.
10. A computer readable storage medium, wherein a clinical drug management program is stored on the computer readable storage medium, and when executed by a processor, the clinical drug management program implements the steps of the clinical drug management 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 |
|---|---|---|---|---|
| CN115954114A (en) * | 2023-03-09 | 2023-04-11 | 一临云(深圳)科技有限公司 | Medicine random coding method, device, equipment and storage medium |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20210366014A1 (en) * | 2017-08-08 | 2021-11-25 | Netorus, Inc. | Method of generating and accessing product-related information |
| CN113808700A (en) * | 2020-06-11 | 2021-12-17 | 阿里健康信息技术有限公司 | Data processing method, device, system and storage medium |
-
2021
- 2021-12-20 CN CN202111557989.2A patent/CN113948164A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20210366014A1 (en) * | 2017-08-08 | 2021-11-25 | Netorus, Inc. | Method of generating and accessing product-related information |
| CN113808700A (en) * | 2020-06-11 | 2021-12-17 | 阿里健康信息技术有限公司 | Data processing method, device, system and storage medium |
Non-Patent Citations (1)
| Title |
|---|
| 崔金栋 等: "基于"互联网+"与云服务的制造型企业生产信息管理机理研究", 《情报科学》 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115954114A (en) * | 2023-03-09 | 2023-04-11 | 一临云(深圳)科技有限公司 | Medicine random coding method, device, equipment and storage medium |
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Application publication date: 20220118 |