CN115187125A - Laboratory data management method, device, equipment and medium - Google Patents
Laboratory data management method, device, equipment and medium Download PDFInfo
- Publication number
- CN115187125A CN115187125A CN202210891089.XA CN202210891089A CN115187125A CN 115187125 A CN115187125 A CN 115187125A CN 202210891089 A CN202210891089 A CN 202210891089A CN 115187125 A CN115187125 A CN 115187125A
- Authority
- CN
- China
- Prior art keywords
- data
- detection
- sample
- laboratory
- submission
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims abstract description 100
- 238000013523 data management Methods 0.000 title claims abstract description 44
- 238000001514 detection method Methods 0.000 claims abstract description 308
- 238000007726 management method Methods 0.000 claims abstract description 67
- 238000003860 storage Methods 0.000 claims abstract description 51
- 238000012550 audit Methods 0.000 claims abstract description 21
- 230000008569 process Effects 0.000 claims description 47
- 238000012360 testing method Methods 0.000 claims description 30
- 238000004590 computer program Methods 0.000 claims description 16
- 238000011084 recovery Methods 0.000 claims description 16
- 238000005070 sampling Methods 0.000 claims description 13
- 238000012795 verification Methods 0.000 claims description 11
- 238000009533 lab test Methods 0.000 claims description 9
- 230000002159 abnormal effect Effects 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 4
- 238000012423 maintenance Methods 0.000 abstract description 15
- 238000007689 inspection Methods 0.000 abstract description 14
- 238000013479 data entry Methods 0.000 abstract description 10
- 230000006870 function Effects 0.000 description 19
- 238000012545 processing Methods 0.000 description 18
- 238000002474 experimental method Methods 0.000 description 12
- 239000002609 medium Substances 0.000 description 12
- 239000003153 chemical reaction reagent Substances 0.000 description 11
- 238000004891 communication Methods 0.000 description 9
- 238000012552 review Methods 0.000 description 9
- 238000011156 evaluation Methods 0.000 description 8
- 238000003908 quality control method Methods 0.000 description 8
- 238000010586 diagram Methods 0.000 description 7
- 238000013439 planning Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- 230000005540 biological transmission Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 230000008859 change Effects 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000012549 training Methods 0.000 description 3
- 230000009471 action Effects 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 231100000481 chemical toxicant Toxicity 0.000 description 2
- 238000013500 data storage Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 230000033772 system development Effects 0.000 description 2
- 239000003440 toxic substance Substances 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 1
- 230000002547 anomalous effect Effects 0.000 description 1
- 238000003491 array Methods 0.000 description 1
- 238000013473 artificial intelligence Methods 0.000 description 1
- 238000013475 authorization Methods 0.000 description 1
- 230000006399 behavior Effects 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000013480 data collection Methods 0.000 description 1
- 230000007123 defense Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000012854 evaluation process Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- -1 kits Substances 0.000 description 1
- 238000011545 laboratory measurement Methods 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 238000010801 machine learning Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 239000013307 optical fiber Substances 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000000275 quality assurance Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012384 transportation and delivery Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06Q—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES; SYSTEMS OR METHODS SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES, NOT OTHERWISE PROVIDED FOR
- G06Q10/00—Administration; Management
- G06Q10/06—Resources, workflows, human or project management; Enterprise or organisation planning; Enterprise or organisation modelling
- G06Q10/063—Operations research, analysis or management
- G06Q10/0633—Workflow analysis
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F16/00—Information retrieval; Database structures therefor; File system structures therefor
- G06F16/30—Information retrieval; Database structures therefor; File system structures therefor of unstructured textual data
- G06F16/31—Indexing; Data structures therefor; Storage structures
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F16/00—Information retrieval; Database structures therefor; File system structures therefor
- G06F16/30—Information retrieval; Database structures therefor; File system structures therefor of unstructured textual data
- G06F16/33—Querying
- G06F16/3331—Query processing
- G06F16/334—Query execution
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F40/00—Handling natural language data
- G06F40/10—Text processing
- G06F40/166—Editing, e.g. inserting or deleting
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F40/00—Handling natural language data
- G06F40/10—Text processing
- G06F40/166—Editing, e.g. inserting or deleting
- G06F40/186—Templates
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06Q—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES; SYSTEMS OR METHODS SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES, NOT OTHERWISE PROVIDED FOR
- G06Q10/00—Administration; Management
- G06Q10/06—Resources, workflows, human or project management; Enterprise or organisation planning; Enterprise or organisation modelling
- G06Q10/063—Operations research, analysis or management
- G06Q10/0639—Performance analysis of employees; Performance analysis of enterprise or organisation operations
- G06Q10/06395—Quality analysis or management
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06Q—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES; SYSTEMS OR METHODS SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES, NOT OTHERWISE PROVIDED FOR
- G06Q10/00—Administration; Management
- G06Q10/10—Office automation; Time management
- G06Q10/103—Workflow collaboration or project management
Abstract
The invention discloses a laboratory data management method, a laboratory data management device, laboratory data management equipment and a laboratory data management medium. A laboratory data management method, comprising: acquiring current submission application data; when the current submission application data passes the audit, determining a sample identifier of the current submission sample; determining the detection plan data of the current submission sample according to the current submission application data and the laboratory detection project management data; and acquiring detection associated data of the current inspection sample according to the detection plan data, and performing data associated storage on the detection associated data and the sample identifier. According to the technical scheme of the embodiment of the invention, the labor cost of data operation and maintenance can be saved, and the accuracy of data entry and the timeliness of data uploading are improved.
Description
Technical Field
The invention relates to the technical field of data processing, in particular to a laboratory data management method, a laboratory data management device, laboratory data management equipment and a laboratory data management medium.
Background
With the increase of laboratory detection items, data needing to be maintained and managed in a laboratory is also increased explosively, and how to effectively manage the laboratory data becomes an important item for laboratory operation and maintenance.
At present, data are mainly maintained and managed by data operation and maintenance personnel in a laboratory, namely, laboratory data are manually input and managed.
The laboratory data volume is huge, and present experimental process data adopts the handwriting record more, and process ageing and sample inspection state can't be tracked in real time, easily leads to data loss, ageing low, is difficult to high-efficient, accurate carry out data logging.
Disclosure of Invention
The invention provides a laboratory data management method, a laboratory data management device, laboratory data management equipment and a laboratory data management medium, which can save the labor cost of data operation and maintenance and improve the accuracy of data entry and the timeliness of data uploading.
According to an aspect of the present invention, there is provided a laboratory data management method including:
acquiring current submission application data;
when the current submission application data passes the verification, determining a sample identifier of the current submission sample;
determining the detection plan data of the current submission sample according to the current submission application data and the laboratory detection project management data;
and acquiring detection associated data of the current sample to be inspected according to the detection plan data, and performing data association storage on the detection associated data and the sample identification.
According to another aspect of the present invention, there is provided a laboratory data management apparatus comprising:
the data acquisition module is used for acquiring current submission application data;
the sample identification determining module is used for determining the sample identification of the current submission sample when the current submission application data passes the auditing;
the system comprises a detection plan data determining module, a data processing module and a data processing module, wherein the detection plan data determining module is used for determining the detection plan data of a current submission sample according to the current submission application data and laboratory detection project management data;
and the data association storage module is used for acquiring detection associated data of the current sample to be inspected according to the detection plan data and storing the detection associated data and the sample identification in a data association manner.
According to another aspect of the present invention, there is provided an electronic apparatus including:
at least one processor; and
a memory communicatively coupled to the at least one processor; wherein the content of the first and second substances,
the memory stores a computer program executable by the at least one processor, the computer program being executable by the at least one processor to enable the at least one processor to perform the laboratory data management method according to any one of the embodiments of the invention.
According to another aspect of the present invention, there is provided a computer-readable storage medium storing computer instructions for causing a processor to perform the laboratory data management method according to any one of the embodiments of the present invention when the computer instructions are executed.
According to the technical scheme of the embodiment of the invention, the sample identification of the current submission sample is determined by acquiring the current submission application data and further determining the detection plan data of the current submission sample when the current submission application data passes the audit, so that the detection associated data of the current submission sample is determined according to the current submission application data and the laboratory detection project management data, the detection associated data of the current submission sample is further acquired according to the detection plan data, and the detection associated data and the sample identification are subjected to data association storage, so that the automatic and intelligent detection planning of the current submission sample is realized, the detection associated data related to the detection link of the current submission sample and the sample identification are subjected to data association storage, the data maintenance of the detection associated data can be facilitated, the problems of data entry errors and data entry untimely are solved because the detection associated data do not need to be manually entered, the problems of high manual cost, poor data entry accuracy and poor data entry timeliness in the prior art due to manual data maintenance in a laboratory are solved, the manual cost of data operation and maintenance can be saved, and the data entry accuracy and the timeliness of data uploading are improved.
It should be understood that the statements in this section do not necessarily identify key or critical features of the embodiments of the present invention, nor do they necessarily limit the scope of the invention. Other features of the present invention will become apparent from the following description.
Drawings
In order to more clearly illustrate the technical solutions in the embodiments of the present invention, the drawings needed to be used in the description of the embodiments will be briefly introduced 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 based on these drawings without creative efforts.
Fig. 1 is a flowchart of a laboratory data management method according to an embodiment of the present invention;
FIG. 2 is a flowchart of a laboratory data management method according to a second embodiment of the present invention;
FIG. 3 is a schematic diagram of a laboratory testing business process according to a second embodiment of the present invention;
fig. 4 is a schematic structural diagram of a laboratory data management apparatus according to a third embodiment of the present invention;
FIG. 5 illustrates a block diagram of an electronic device that may be used to implement embodiments of the invention.
Detailed Description
In order to make those skilled in the art better understand the technical solutions of the present invention, the technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be obtained by a person skilled in the art without making any creative effort based on the embodiments in the present invention, shall fall within the protection scope of the present invention.
It should be noted that the terms "initial", "target", and the like in the description and claims of the present invention and in the drawings described above are used for distinguishing between similar elements and not necessarily for describing a particular sequential or chronological order. It is to be understood that the data so used is interchangeable under appropriate circumstances such that the embodiments of the invention described herein are capable of operation in sequences other than those illustrated or described herein. Moreover, the terms "comprises," "comprising," and "having," and any variations thereof, are intended to cover a non-exclusive inclusion, such that a process, method, system, article, or apparatus that comprises a list of steps or elements is not necessarily limited to those steps or elements expressly listed, but may include other steps or elements not expressly listed or inherent to such process, method, article, or apparatus.
Example one
Fig. 1 is a flowchart of a laboratory data management method according to an embodiment of the present invention, where the embodiment is applicable to a situation of performing efficient operation and maintenance on laboratory data, and the method may be performed by a laboratory data management apparatus, where the laboratory data management apparatus may be implemented in a form of hardware and/or software, and the laboratory data management apparatus may be configured in an electronic device. As shown in fig. 1, the method includes:
and S110, acquiring the current submission application data.
The current submission application data may be related data provided during the current sample submission. Optionally, the current submission application data includes submission person information, a submission sample type, submission time, a detection type, and the like.
In the embodiment of the invention, the current submission application data needs to be acquired, and then the detection plan of the submission sample is formulated according to the current submission application data.
And S120, when the current submission application data is approved, determining the sample identifier of the current submission sample.
The current submission sample may be a submission sample corresponding to the current submission application data. The sample identifier may be an identifier assigned to the censored sample, and is used for distinguishing different censored samples. The sample identifications of different submission samples are different. The sample identification may be two-dimensional code, bar code, etc.
In the embodiment of the present invention, after the current submission application data is obtained, content verification (such as data integrity, normative verification, and the like) may be performed on the current submission application data, and then a sample identifier is assigned to the current submission sample corresponding to the current submission application data that passes the verification.
And S130, determining the detection plan data of the current submission sample according to the current submission application data and the laboratory detection project management data.
The laboratory test item management data may be management data related to the declared test items, and is used for determining test time of the declared test items and test equipment required by each test item. The detection plan data may be data describing a detection plan for the submitted sample. The test schedule data may include the scheduled test time for the sample being tested, the required test equipment, etc.
In the embodiment of the invention, the detection project of the current submission sample corresponding to the current submission application data can be determined according to the current submission application data, and then the detection plan of the current submission sample is formulated according to the laboratory detection project management data and the determined detection project of the current submission sample, so that the detection plan data of the current submission sample is obtained.
S140, acquiring detection associated data of the current sample to be detected according to the detection plan data, and performing data association storage on the detection associated data and the sample identification.
Wherein the detection-related data may be data associated with a detection process of the censored sample. The detection-related data may include, but is not limited to, detection equipment, sample detection video, sample detection results, detection personnel information, time for obtaining detection results, and the like
In the embodiment of the invention, the scheduled detection time of the current submission sample can be determined according to the detection scheduled data, the detection associated data of the current submission sample can be automatically obtained in real time at the scheduled detection time of the current submission sample, the association between the submission associated data and the sample identifier of the current submission sample is established, and the data association storage is further carried out on the detection associated data and the sample identifier.
According to the technical scheme, the sample identification of the current submission sample is determined by acquiring the current submission application data and further determining the detection plan data of the current submission sample when the current submission application data passes the auditing, so that the detection associated data of the current submission sample is determined according to the current submission application data and the laboratory detection project management data, and the detection associated data of the current submission sample is further acquired according to the detection plan data and is subjected to data association storage with the sample identification, so that the automatic and intelligent detection planning of the current submission sample is realized, and the detection associated data related to the detection link of the current submission sample and the sample identification are subjected to data association storage, so that the data maintenance of the detection associated data can be facilitated.
Example two
Fig. 2 is a flowchart of a laboratory data management method according to a second embodiment of the present invention, and this embodiment provides a specific alternative implementation manner for determining the detection plan data of the current submission sample according to the current submission application data and the laboratory detection project management data based on the second embodiment. As shown in fig. 2, the method includes:
and S210, acquiring current submission application data.
And S220, when the current submission application data passes the verification, determining the sample identifier of the current submission sample.
And S230, determining the detection arrangement time and the detection equipment data of the historical unprocessed submission sample matched with the historical unprocessed submission application data according to the laboratory detection project management data.
The historical unprocessed submission application data may be the submission application data of the submission sample that has completed the application of the detection item of the submission sample, but has not yet been detected. The historical unprocessed submission sample may be a submitted submission application data, but not a submitted submission sample for detection. The scheduled time for detection may be a scheduled time for detection of the submitted sample. The test device data can be data related to the device that tested the sample under test. The detection device data may include the model of the device, the type of item detected by the device, the time at which the device detected, and so on.
In the embodiment of the invention, the historical unprocessed submission application data can be obtained first, so that the historical unprocessed submission samples matched with the historical unprocessed submission application data are determined, the laboratory test item management data are analyzed, and the test arrangement time and the test equipment data of the historical unprocessed submission samples are determined.
In an optional embodiment of the present invention, before determining, according to the laboratory test item management data, a scheduled detection time and detection equipment data of the historical unprocessed submission samples matching the historical unprocessed submission application data, the method may further include: acquiring detection standard updating data, equipment identification data and historical unprocessed submission application data; and determining laboratory test item management data according to the test standard update data, the equipment identification data and the historical unprocessed submission application data.
The detection standard updating data can be used for adjusting and updating the detection standard of the detection item. The device identification data may be device identification data of the detection devices for distinguishing between different detection devices.
In the embodiment of the invention, the detection standard updating data can be obtained in real time, the equipment identification data of the current normal equipment in the laboratory and the historical unprocessed submission application data are obtained, and then the detection items of the historical unprocessed submission samples are planned and managed by using the detection standard updating data, the equipment identification data of the normal equipment and the historical unprocessed submission application data which are obtained in real time, so as to obtain the laboratory detection item management data.
And S240, determining the detection plan data of the current submission sample according to the detection scheduled time of the historical unprocessed submission sample and the detection equipment data.
In the embodiment of the invention, after the detection scheduling time and the detection equipment data of the historical unprocessed submission sample are obtained, the current submission application data is analyzed to determine the detection equipment required by the detection item of the current submission sample, and then the detection plan data of the current submission sample is formulated according to the detection scheduling time and the detection equipment data of the historical unprocessed submission sample and the detection equipment required by the detection item of the current submission sample.
And S250, acquiring detection associated data of the sample to be detected according to the detection plan data, and performing data association storage on the detection associated data and the sample identification.
In an optional embodiment of the present invention, acquiring detection associated data of a current sample to be examined according to the detection plan data, and performing data association storage on the detection associated data and a sample identifier may include: acquiring detection result data according to the detection plan data; performing at least one audit on the detection result data to obtain audit record data; and performing data association storage on the detection result data, the audit record data and the sample identifier.
Wherein the detection result data may be data characterizing the detection result of the sample under examination. The audit record data may be data recorded when the detection result data is audited. The audit record data may include audit staff information, audit results (audit passed or audit failed) of the detection result data, and the like.
In the embodiment of the invention, the scheduled detection time of the current submission sample can be determined according to the detection result data, so that the detection associated data of the current submission sample can be obtained in real time according to the scheduled detection time, when the detection result data exists in the detection associated data, the detection result data is further audited at least once, the data associated with the auditing process is recorded and used as the auditing record data, the detection result data and the auditing record data are respectively associated with the sample identifier of the current submission sample, and the detection result data, the auditing record data and the sample identifier are subjected to data association storage.
In an optional embodiment of the present invention, after the data association storing the detection association data and the sample identifier, the method may further include: when the detection result data passes the audit, generating an initial detection report according to the detection result data; and editing the initial detection report according to the report language support type to generate a target detection report, and sending the target detection report to a target user.
Wherein the initial detection report may be a detection report generated according to the detection result data and the report template. The report language support type may be a language type of detection report support set in advance. The target detection report can edit the initial detection report according to the report language support type. The target user may be the user who provided the current submission application data.
In the embodiment of the invention, after the detection result data is obtained, the detection result data can be audited, when the detection result data is audited, the detection result data can be input into a report template matched with the current detection application data to generate an initial detection report, the initial detection report is further edited according to the support type of the report language and the text display language selected by a target user to generate a target detection report, and the target detection report is further sent to the target user through the existing file transmission form.
In an optional embodiment of the present invention, after sending the target detection report to the target user, the method may further include: acquiring feedback data of a target user to a target detection report; when the feedback data are abnormal feedback data, obtaining detection process tracing data; and tracing the detection process to data and sending the data to a target user.
The feedback data may be feedback information sent by the target user and reported to the target detection. The anomalous feedback data may be data characterizing the objection of the target user to the target detection report. The inspection process traceability data may be data characterizing the inspection process of the current sample under inspection.
In the embodiment of the invention, after the target detection report is sent to the target user, the feedback data of the target user to the target detection report can be further acquired, if the feedback data is abnormal feedback data, namely the target user says that the target detection report is objected, the detection process tracing data can be further collected and sent to the target user, so that the target user can check the detection process of the current submission sample. If the feedback data is non-abnormal feedback data, namely the target user does not have objection to the target detection report, the retroactive data in the detection process does not need to be collected and forwarded.
Optionally, the target user may supervise data associated with the testing process in the process tracing data, and indicate an operation that is not compliant in the testing process, and it is understood that laboratory managers may also audit the testing process based on recorded videos, recorded texts, and the like of the testing process, so as to ensure compliance of the testing process.
In an optional embodiment of the present invention, after performing data association storage on the detection association data and the sample identifier, the method may further include: acquiring sampling recovery sample data; and performing data association storage on the sampling recovery sample data and the sample identification, and sending the sampling recovery sample data to a target user.
The sample recovery sample data may be related data representing a sample remaining sample before the current sample to be inspected is detected. The sample recovery sample data may include, but is not limited to, a sample type of the sample left, administrator information of the sample left, a laboratory where the sample left is stored, and the like.
In the embodiment of the invention, the sample recovery and sampling data can be subjected to data storage before the current inspection sample is detected, and then the sample recovery and sampling data and the sample identification are subjected to data association storage after the detection associated data and the sample identification are subjected to data association storage, so that when a target detection report is sent to a target user, the sample recovery and sampling data can also be sent to the target user.
Fig. 3 is a schematic diagram of a laboratory detection service process according to a second embodiment of the present invention, and as shown in fig. 3, the laboratory detection service process includes: the method comprises the steps of dispatching a order to log in a system (a data management system for executing a laboratory data management method), dispatching the order and generating a two-dimensional code, sampling according to the order by a sampling person, delivering a detected sample to a laboratory, receiving an application and verification item (a detection item corresponding to the delivery and detection application data) by the laboratory, identifying a sample, inputting the sample (scanning the code), determining detection equipment (scanning the code), receiving the detection data, generating a detection report, submitting the report for verification, recovering the sample and informing the receiving of the detection report, and determining the report and evaluating service by a consignor. According to the actual detection business process of a laboratory, the circulation of the detection business in the system is realized through a workflow mechanism, and the whole process from entrusted handling to report filing is supported. In the testing process, the laboratory working efficiency is improved by the automatic functions of automatic calculation, automatic reduction, automatic judgment, automatic generation of original records, automatic generation of testing reports and the like from the data acquisition of the testing instrument. The inspection business process is customized through the workflow mechanism, and the change can be conveniently realized according to the change of the inspection process. And each step of auditing action of the system workflow strictly adopts mechanisms such as electronic signature and the like. In the whole process, each link stores data, and when different users are faced, the data information inquired by the users is different and is defined according to the authority of the users.
The system is realized by adopting a three-layer architecture, namely: interface, service and data, the interface layer and service layer of the system are separated from each other, and no matter the interface layer is changed or the service layer is changed, the interface layer and service layer can be not influenced with each other, thereby being beneficial to the maintenance and function expansion of the system and enhancing the flexibility of the system; the service logic is implemented on the application server, rather than on each client. The access to the data can be only carried out through the application server, so that the safety of the system is enhanced, and a thin client is realized; the data needed by the client can be pre-processed or fully processed in the application server, and then the processing result is transmitted to the client, so that the network communication volume is reduced. According to the analysis result of the user requirement in the early stage, the system is used for carrying out all-around management on a laboratory and mainly comprises a detection business process module, a laboratory resource management module and an experimental quality control module. The detection service flow process module realizes quick and convenient management flow mainly aiming at laboratory detection service, and can automatically collect data in the process so as to reduce experiment errors. The laboratory resource management module is mainly used for carrying out comprehensive information management on laboratory staff, laboratory instruments, detection items, resources, clients and the like of a detection room. The experiment quality control module is mainly used for establishing various types of quality control plans aiming at quality safety risk defense of each stage of experiment activities.
The consignor can be automatically authorized to log in the system, the system can automatically read the identity information of the current user, and the consignor initiates an application to request for detection of a submission sample and give a detailed detection report after authorization. The consignor needs to add a new consignment application (equivalent to submission application data) after logging in the system, can delete the existing consignment application in a useless way, and can modify the existing consignment application through simple copy operation so as to achieve the purpose of quick application. Meanwhile, the consignor can perform a query function on the consignment application, and conveniently and quickly refers to and browses the contents of the consignment application. Meanwhile, one entrusting application form can be applied to detect a plurality of inspection samples, the inspection samples can also correspond to a plurality of inspection items, and the content of the entrusting application form needs to be enriched and detailed as far as possible.
And for the newly received request application in the laboratory, the laboratory can be used for detecting the samples to be checked after the request application is checked. In the stage, the normative examination of the application is mainly carried out by laboratory service personnel, and the laboratory service personnel completely include the content authority of the application. When the laboratory chief reviews the application, the examination content of the application, the required laboratory environment, the required equipment and other information are reviewed, so that the examination right of the application of the laboratory chief is directed to the examination content.
After the commission application is approved, the laboratory chief makes an experimental arrangement on the detection content of the application. At this stage, arrangement recommendation is given according to the detection period of the project by aiming at information systems such as large equipment information and related staff information used by the detection project on the application form, personnel, equipment and scheduling are selected by a laboratory manager, and the system automatically informs the related staff to carry out experiment preparation.
After the consignor sends the sample, the laboratory signs the sample and receives the sample information to be put in storage. At the stage, the system can generate sample identification of the sample, and a bar code, a two-dimensional code and an RFID mode can be adopted. The user can modify the information of the sample and can supplement the storage position of the sample.
Before the experiment, to laboratory measurement personnel and laboratory supplies administrator, the sample administrator carries out the experiment and prepares to remind, accomplishes the preliminary period preparation work that detects the project.
After the laboratory detector detects the sample conveying sample, the detection result data can be automatically imported into the system, so that secondary manual operation is avoided as much as possible. In the stage, a sample inspector not only needs to record the detection result data of the samples to be inspected into the system, but also needs to record the information of the used equipment into the system, the automatic recording is realized by scanning the two-dimensional code information of the equipment, and the equipment information is not recorded, so that the detection result is regarded as incomplete and cannot be submitted to the next link for evaluation.
And after the sample inspector inputs the detection result into the system, the same group of workers are reminded to make evaluation on the detection result and submit an evaluation record. If the examination is passed, the sample inspector can enter the next link to generate a detection report for the sample, and secondary detection is required if the examination is not passed.
The detection of the samples to be checked is completed, and the laboratory needs to give an authoritative sample report. In the stage, the system can realize online detection report editing, report modification and report query. The system can automatically apply the existing report style according to the experimental detection type and the sample category of the sample to generate an experimental detection report, the report supports Chinese and English, a special detection seal can be added, and meanwhile, a user can edit and modify the report on line and support report preview. The report can not be modified by the user without permission to the generated and passed report.
And the laboratory manager receives the detection report submitted by the laboratory inspector, checks the report on line, and passes the electronic signature verification after confirming the error. The user can retrieve and group reports by date.
After the test report is approved, the system will alert the sample administrator and customer to code for sample recovery.
After the examination and verification of the detection report are passed, a laboratory salesman can send the detection report to a mailbox of a client of the client through a system mail platform, and simultaneously, information such as email time, salesman name, mailbox address and the like of the report is automatically generated in the system and stored in a warehouse. The clerk can also post the report to the consignor address by printing the report on a lab-specific stamp. The mobile terminal of the entrusting party can receive the information issued by the report and open the link through the password to directly check the detection report.
The laboratory resource management module manages basic resources of a laboratory, including information management of personnel, equipment, suppliers and the like, and information management of detection methods, detection standards and the like related to experimental projects, so that the laboratory resources can be conveniently and quickly used. The method specifically comprises the following steps: 1. the personnel management module can carry out comprehensive and informationized management on the personnel information of the laboratory, including the storage of the basic information of the personnel and the management of the change of the position information. Laboratory test technicians must be trained to go on duty, and therefore necessary updating management needs to be carried out on training information of the personnel in the module, and information such as training certificates and grade certificates of the personnel can be uploaded. The management of the personnel information is mainly performed by the staff of the functional department, and other staff can only modify the basic information of the staff. 2. The equipment management not only comprehensively manages basic information of the equipment, but also comprises unified planning management of maintenance information, purchase information and purchase application of the equipment. The system can print the identification of the equipment, check the service condition and state information of the equipment, and count the frequency of equipment experiments. 3. The laboratory will do the sample processing to the censored sample, need to modify the basic information of sample at this sample management module, add performance information that its detected etc.. Meanwhile, the whole life cycle of the sample is comprehensively tracked and processed. After receiving the sample, the laboratory encodes the sample through the system, and the sample is combined with the bar code, so that the sample can be conveniently scanned and tracked. 4. The system supports information maintenance of a laboratory detection method and a detection standard, and tracking records are made on an updated version of the laboratory detection method and the detection standard, so that a user can conveniently search and use the laboratory detection method and the detection standard. The system in the module supports uploading of related files, supports a user to directly look up the files in the system for learning, can set authority information of the files, records and tracks revision information of the user, automatically cleans expired files and can retrieve and inquire the files. 5. The system should carry out unified code management to the detection project in laboratory. The system should conform to two completely different patterns of detection, serialized and non-serialized. The test items include information on a test method used in the item, a method for calibration of the test, equipment required for performing the item, and necessary reagents and supplies required for the experiment. The laboratory detection items are set and managed in advance, the experimental process is modeled and standardized, and the detection accuracy is improved. The detection method in the detection item can make online modification on the information of the method, including information of a calculation formula, an important index parameter, a graphic illustration and the like. The system in the functional module can help a laboratory to quickly construct a new detection room through the standardized management of detection items, and the operation is conveniently and quickly performed. 6. The system manages the suppliers not only by storing and processing basic information, but also stores and manages the certification documents of the suppliers in a laboratory, and provides the uploading function of the user documents. Meanwhile, the system should provide storage management for evaluation information, observation information, goods registration information and price record information of suppliers, and make selection judgment conveniently when supplies such as follow-up purchasing equipment, reagents and the like are used. The capability certification document of the supplier comprises certificates of legal operation, contract agreement with a laboratory, service specification certification and the like. 7. A file management module of the system mainly aims at uploading normative files in the production and operation process of a laboratory to perform storage management, and the normative files comprise quality assurance files of the laboratory, laboratory management standard files, activity rule files of the laboratory, technical file information of the laboratory and the like. The file management process needs to follow the CNAS requirements and perform whole-process tracking and monitoring on drafting, announcement, revision, review and version update of the file. Meanwhile, the system can set the reading authority of the file. Laboratory inspectors can view the corresponding normative document information while in the process of detection. 8. Scientific and efficient consumable management is a powerful guarantee for ensuring that a laboratory develops daily detection work and improving detection quality. The laboratory should make sure the safety person responsible for the consumables, establish a health acceptance system, and make corresponding procedures of purchasing, keeping and using and corresponding assessment systems. The consumable material using department must make clear the safety responsibility and consumable material management personnel of the department. The experiment consumable comprises reagent consumables and non-reagent consumables. The reagent type consumable includes: chemical reagents, reference reagents, standard substances, laboratory water, microorganism culture media, kits, solutions or solid mixtures prepared from related reagents, and the like. The non-reagent consumable includes: glassware, experimental gas, special consumable materials for instruments, filter paper, rubber products and the like. The inspection consumables have dangerous characteristics of explosion, flammability, poison, infection, corrosion, radioactivity and the like, and articles and toxic-making chemicals which need special protection are easily caused to human casualties, property damages or environmental pollution in transportation, storage, use and treatment to become dangerous articles. The catalog of dangerous articles is determined according to GB6944 "Classification and name number of dangerous articles and goods", catalog of highly toxic chemicals "and" catalog of Classification and variety of easily toxic chemicals ". After the consumables are put in storage, sorting and arrangement are carried out, and a reception record is registered, so that the consumables are prevented from being discarded due to overdue placement, and the loss caused by expense is avoided.
The functional points of the laboratory resource management module comprise: adding new laboratory employee information; the basic information of the staff is modified (when the current user is the staff, only the personal basic information can be modified, and the user has no right to modify for reward and punishment conditions and training conditions); the method comprises the steps of deleting functions (the deleting function can only delete employee accessory information, other information cannot be deleted after confirmation submission, inquiring functions (the inquiry of employee information adopts employee job numbers and employee names as key words), displaying information (the display of interface employee information is displayed according to division of departments), uploading accessory information (a user can upload information such as establishment and health certification, the uploading format is PDF, judgment is made on the file format uploaded by the user, and reminding is touched when the format is wrong).
When the function point is realized, firstly, the UI layer empeleForm receives a user request, the user request processing information is sent to the service logic layer empeleBLL, the service logic layer interacts with the database access layer, the database access layer DAO interacts with the data source to acquire data from the database, the data are fed back to the service logic layer step by step, the empeleBLL processes the data and then returns the data to the UI layer, and the UI layer displays the information to the user.
The laboratory resource management module may further include a consumable center management function point, including: and (4) consumable classification: managing classification information of consumables; consumable item list: managing a consumable list, wherein consumable information cannot be directly updated in the consumable list, and management is performed through warehousing and ex-warehousing; warehousing: warehousing consumables (adding consumables into a consumable list at the same time), managing warehousing records, and adding a plurality of consumables in one-time warehousing; newly establishing a consumable record (some consumables may have valid time limit) every time the consumables are put in storage; recycling consumables: after the experiment, if there is excess consumable material that can be recycled, it is recycled. The process comprises the following steps: submitting a report-administrator auditing (pass) -inspecting consumables (removing unrecoverable, modifying the report) -confirming warehousing-end; and (4) ex-warehouse: the consumables are delivered out of the warehouse (simultaneously subtracted from the consumables list), the ex-warehouse record is managed, and a plurality of consumables can be taken out in one-time warehousing; purchase application: the user submits a consumable purchase application and a high-level administrator checking and processing request, and the process comprises the following steps: the user provides an application, a laboratory captain checks the processing application, audits feedback and finishes processing. The precondition of the consumable central management function point is that laboratory detection personnel and laboratory managers apply for purchasing, using and auditing the consumables to be put in and out of a warehouse.
The laboratory consumables may include reagent-based consumables and non-reagent-based consumables. The laboratory should be clear of the safety responsible person of the laboratory and the management department of the inspection consumables. The management department should make corresponding procedures of purchasing, keeping and using and corresponding assessment system. The consumable material using department should make clear the safety responsibility and consumable material manager of the department.
The experimental quality control module can analyze the control requirements of a quality system, and comprises the following steps: 1. the project schedule control is that laboratory managers initiate to make project plans, and the project plans enter a checking link after being submitted. In the module, past project plans can be inquired, and the implementation condition of the project plans can be recorded and tracked. 2. The evaluation comprises evaluation process management and evaluation noncompliant project management. The system supports management personnel to carry out project planning in advance and send the planning to relevant personnel to enter an approval process. After the project plan is submitted, the system reminds workers to check the project plan, and the system supports uploading of a review file and information such as meeting minutes of related meetings after review. And recording the project which is not passed by the evaluation, correcting and tracking the progress in real time to ensure the smooth promotion of the project plan. 3. The method is mainly used for receiving user evaluation information and providing a user complaint entrance. If the customer has any question and question about the detection result, a complaint can be proposed, and after receiving the system complaint prompt, if the complaint is accepted, the whole detection process needs to be traced again and the result needs to be fed back to the customer. 4. Quality control is focused on three major aspects, including uncertainty management control, device duration verification, and data table generation. The uncertainty is mainly controlled by calibrating the detection result of the standard instrument, mainly by maintaining the standard certificate and the auxiliary instrument device of the standard instrument. The equipment period checking is to set an equipment checking period and remind a worker to maintain, and a maintenance statistical report is generated. The data table is mainly used for carrying out visual management on data generated by experiments, a set of unified data table is generated, the data table comprises median, a stable variation coefficient and the like, and the generated data can be inquired.
The user service function point of the experimental quality control module can comprise: recording the complaints of the users; deleting the user complaint record (deleting and re-uploading the attachable information); submitting a user complaint record; uploading the attachment information; and checking historical complaints. The precondition of the user service function point is that the record is deleted and the record state is required to be an uncommitted state; the format of the attachment information is PDF or JPG; and when the complaint records are newly added, the current user role is the functional customer service.
The project scheduling module and the review module in the laboratory quality control module have certain relevance. Firstly, a user submits a new project plan arrangement application to enter a review link after entering a project arrangement module. At this time, a new record is added in the project table of the database, and the initial status is 0, the user submits after confirming that the plan is completely written, and the update status field information is 1. And submitting the project to enter a review link. The related personnel can see the project plan after entering the review module, the project state information of the database is updated after the review is passed, the user with the user role of quality control personnel can see the project information after logging in the module, the prevention is completed, and the project tracking is started after the correction information is corrected.
The system can automatically collect and analyze data, instrument equipment is required to be connected with the system in the aspect of automatic data collection, detection result data are input into the system through a special information transmission pipeline, and secondary errors caused by manual input are avoided. The expansion of laboratory business scale requires purchasing a large amount of new equipment, and for serial port type equipment or other interface equipment, connection configuration is firstly required when the equipment is integrated with a system, and the function mainly provides a uniform window for instrument connection configuration.
The data acquisition mainly comprises the steps of importing experimental result data into a system from instrument equipment in a real-time automatic mode, and checking, acquiring and storing the data in real time. In the function, a user can trigger by one key according to requirements, the experimental result is imported into an interface to be checked, and the experimental result information is stored after the experimental result information is confirmed to be correct. The laboratory equipment is numerous, and the inspector can not examine the operational aspect of laboratory equipment every time the experiment begins, under this function in view of this kind of condition, the system all has the function of examining laboratory equipment operational aspect (equipment running state, unusual trigger etc.) in real time.
The system does not restrict the authorized registration of users according to the needs of the laboratory business expansion. The system response time does not exceed 2 seconds; the effective time for logging data is within 5 seconds. The response time of the list table should be within 5 seconds when the system performs the query search operation, and the feedback time for the special data should not exceed 5 seconds. For sudden system failure, a system database should have a backup scheme, and system settings can be restored in a short time. The system operation environment should be safe and reliable, the normal operation of the system is guaranteed, and the request operation of a large amount of data for a long time can be met. The system has certain stability, can store the data in a laboratory for a long time, and can perform regular backup processing on the database data, so that the safety of the data is guaranteed, and meanwhile, the data has certain traceability. The system data processing should have confidentiality to prevent information leakage. In addition, the system should grant a corresponding unique electronic signature to laboratory staff, and the data of the electronic signature is verified by the system through a public key so as to ensure the validity and validity of the electronic signature. The system has friendly interface, is convenient for the user to operate, the user can clearly know the function of each interface, online help is provided in each module, and the user can freely configure according to the behavior habit of the user when necessary. The system can integrate management with technology. The management system of the laboratory and the future development and planning are reasonably integrated in the system development process. Meanwhile, the system can be compatible with an old-time system and a future application system, and can be highly engaged and fused with a universal data source. The system should have good maintainability, so that when a bug defect occurs in later system operation, a maintainer can quickly deal with the problem, and the soundness of a system development design document is ensured as much as possible.
According to the technical scheme, the sample identification of the current submission sample is determined by acquiring the current submission application data, the detection arrangement time and the detection equipment data of the historical unprocessed submission sample matched with the historical unprocessed submission application data are determined according to laboratory detection project management data, the detection plan data of the current submission sample are determined according to the detection arrangement time and the detection equipment data of the historical unprocessed submission sample, the detection associated data of the submission sample are acquired according to the detection plan data, and the detection associated data and the sample identification are stored in a data association mode, so that the automatic and intelligent detection plan of the current submission sample is realized, the detection associated data related to the detection link of the current submission sample and the sample identification are stored in a data association mode, the data maintenance of the detection associated data can be facilitated, the problems of data entry errors and data entry failure in time are avoided due to the fact that the detection associated data do not need to be manually entered, the problems of high manual cost, poor data entry accuracy and poor data uploading accuracy of the laboratory data are solved, and the efficiency of data transmission is improved.
In the technical scheme of the embodiment of the invention, the acquisition, storage, application and the like of the related personal information (such as personnel information and the like) accord with the regulations of related laws and regulations without violating the common customs of public order.
EXAMPLE III
Fig. 4 is a schematic structural diagram of a laboratory data management apparatus according to a third embodiment of the present invention. As shown in fig. 4, the apparatus includes:
a data obtaining module 310, configured to obtain current submission application data;
a sample identifier determining module 320, configured to determine a sample identifier of the current submission sample when the current submission application data passes the audit;
a detection plan data determining module 330, configured to determine detection plan data of a current submission sample according to current submission application data and laboratory detection project management data;
and the data association storage module 340 is configured to obtain, according to the detection plan data, detection association data of the current inspection sample according to the detection plan data, and perform data association storage on the detection association data and the sample identifier.
According to the technical scheme, the sample identification of the current submission sample is determined by acquiring the current submission application data and further determining the detection plan data of the current submission sample when the current submission application data passes the auditing, so that the detection associated data of the current submission sample is determined according to the current submission application data and the laboratory detection project management data, and the detection associated data of the current submission sample is further acquired according to the detection plan data and is subjected to data association storage with the sample identification, so that the automatic and intelligent detection planning of the current submission sample is realized, and the detection associated data related to the detection link of the current submission sample and the sample identification are subjected to data association storage, so that the data maintenance of the detection associated data can be facilitated.
Optionally, the detection plan data determining module 330 is configured to determine, according to the laboratory detection project management data, a detection schedule time and detection device data of the historical unprocessed submission sample that are matched with the historical unprocessed submission application data; and determining the detection plan data of the current submission sample according to the detection scheduling time and the detection equipment data of the historical unprocessed submission sample.
Optionally, the laboratory data management apparatus further includes a laboratory test item management data obtaining module, configured to obtain test standard update data, device identification data, and the historical unprocessed submission application data; and determining the laboratory test item management data according to the test standard updating data, the equipment identification data and the historical unprocessed submission application data.
Optionally, the data association storage module 340 is configured to obtain detection result data according to the detection plan data; performing at least one audit on the detection result data to obtain audit record data; and performing data association storage on the detection result data, the audit record data and the sample identifier.
Optionally, the laboratory data management apparatus further includes a target detection report sending module, configured to generate an initial detection report according to the detection result data when the examination of the detection result data is passed; and editing the initial detection report according to the report language support type to generate a target detection report, and sending the target detection report to a target user.
Optionally, the laboratory data management device further includes a detection process tracing data sending module, configured to obtain feedback data of the target user on the target detection report; when the feedback data are abnormal feedback data, obtaining detection process tracing data; and sending the detection process tracing data to the target user.
Optionally, the laboratory data management device further includes a sample recovery and sample data storage and transmission module, configured to obtain sample recovery and sample data; and performing data association storage on the sampling recovery sample data and the sample identification, and sending the sampling recovery sample data to the target user.
The laboratory data management device provided by the embodiment of the invention can execute the laboratory data management method provided by any embodiment of the invention, and has the corresponding functional modules and beneficial effects of the execution method.
Example four
FIG. 5 illustrates a schematic diagram of an electronic device that may be used to implement embodiments of the present invention. Electronic devices are intended to represent various forms of digital computers, such as laptops, desktops, workstations, personal digital assistants, servers, mainframes, and other appropriate computers. The electronic equipment may also represent various forms of mobile devices, such as personal digital processing computing devices and the like. The components shown herein, their connections and relationships, and their functions, are meant to be exemplary only, and are not meant to limit implementations of the inventions described and/or claimed herein.
As shown in fig. 5, the electronic device 10 includes at least one processor 11, and a memory communicatively connected to the at least one processor 11, such as a Read Only Memory (ROM) 12, a Random Access Memory (RAM) 13, and the like, wherein the memory stores a computer program executable by the at least one processor, and the processor 11 can perform various suitable actions and processes according to the computer program stored in the Read Only Memory (ROM) 12 or the computer program loaded from a storage unit 18 into the Random Access Memory (RAM) 13. In the RAM 13, various programs and data necessary for the operation of the electronic apparatus 10 can also be stored. The processor 11, the ROM 12, and the RAM 13 are connected to each other via a bus 14. An input/output (I/O) interface 15 is also connected to the bus 14.
A number of components in the electronic device 10 are connected to the I/O interface 15, including: an input unit 16 such as a keyboard, a mouse, or the like; an output unit 17 such as various types of displays, speakers, and the like; a storage unit 18 such as a magnetic disk, an optical disk, or the like; and a communication unit 19 such as a network card, modem, wireless communication transceiver, etc. The communication unit 19 allows the electronic device 10 to exchange information/data with other devices via a computer network such as the internet and/or various telecommunication networks.
In some embodiments, the laboratory data management method may be implemented as a computer program tangibly embodied in a computer-readable storage medium, such as storage unit 18. In some embodiments, part or all of the computer program may be loaded and/or installed onto the electronic device 10 via the ROM 12 and/or the communication unit 19. When the computer program is loaded into RAM 13 and executed by processor 11, one or more steps of the laboratory data management method described above may be performed. Alternatively, in other embodiments, the processor 11 may be configured to perform the laboratory data management method by any other suitable means (e.g., by means of firmware).
Various implementations of the systems and techniques described here above may be implemented in digital electronic circuitry, integrated circuitry, field Programmable Gate Arrays (FPGAs), application Specific Integrated Circuits (ASICs), application Specific Standard Products (ASSPs), system on a chip (SOCs), load programmable logic devices (CPLDs), computer hardware, firmware, software, and/or combinations thereof. These various embodiments may include: implemented in one or more computer programs that are executable and/or interpretable on a programmable system including at least one programmable processor, which may be special or general purpose, receiving data and instructions from, and transmitting data and instructions to, a storage system, at least one input device, and at least one output device.
Computer programs for implementing the methods of the present invention can be written in any combination of one or more programming languages. These computer programs may be provided to a processor of a general purpose computer, special purpose computer, or other programmable data processing apparatus, such that the computer programs, when executed by the processor, cause the functions/acts specified in the flowchart and/or block diagram block or blocks to be performed. A computer program can execute entirely on a machine, partly on the machine, as a stand-alone software package, partly on the machine and partly on a remote machine or entirely on the remote machine or server.
In the context of the present invention, a computer-readable storage medium may be a tangible medium that can contain, or store a computer program for use by or in connection with an instruction execution system, apparatus, or device. A computer readable storage medium may include, but is not limited to, an electronic, magnetic, optical, electromagnetic, infrared, or semiconductor system, apparatus, or device, or any suitable combination of the foregoing. Alternatively, the computer readable storage medium may be a machine readable signal medium. More specific examples of a machine-readable storage medium would include an electrical connection based on one or more wires, a portable computer diskette, a hard disk, a Random Access Memory (RAM), a read-only memory (ROM), an erasable programmable read-only memory (EPROM or flash memory), an optical fiber, a compact disc read-only memory (CD-ROM), an optical storage device, a magnetic storage device, or any suitable combination of the foregoing.
To provide for interaction with a user, the systems and techniques described here can be implemented on an electronic device having: a display device (e.g., a CRT (cathode ray tube) or LCD (liquid crystal display) monitor) for displaying information to a user; and a keyboard and a pointing device (e.g., a mouse or a trackball) by which a user may provide input to the electronic device. Other kinds of devices may also be used to provide for interaction with a user; for example, feedback provided to the user can be any form of sensory feedback (e.g., visual feedback, auditory feedback, or tactile feedback); and input from the user may be received in any form, including acoustic, speech, or tactile input.
The systems and techniques described here can be implemented in a computing system that includes a back-end component (e.g., as a data server), or that includes a middleware component (e.g., an application server), or that includes a front-end component (e.g., a user computer having a graphical user interface or a web browser through which a user can interact with an implementation of the systems and techniques described here), or any combination of such back-end, middleware, or front-end components. The components of the system can be interconnected by any form or medium of digital data communication (e.g., a communication network). Examples of communication networks include: local Area Networks (LANs), wide Area Networks (WANs), blockchain networks, and the internet.
The computing system may include clients and servers. A client and server are generally remote from each other and typically interact through a communication network. The relationship of client and server arises by virtue of computer programs running on the respective computers and having a client-server relationship to each other. The server can be a cloud server, also called a cloud computing server or a cloud host, and is a host product in a cloud computing service system, so that the defects of high management difficulty and weak service expansibility in the traditional physical host and VPS service are overcome.
It should be understood that various forms of the flows shown above may be used, with steps reordered, added, or deleted. For example, the steps described in the present invention may be executed in parallel, sequentially, or in different orders, and are not limited herein as long as the desired results of the technical solution of the present invention can be achieved.
The above-described embodiments should not be construed as limiting the scope of the invention. It should be understood by those skilled in the art that various modifications, combinations, sub-combinations and substitutions may be made in accordance with design requirements and other factors. Any modification, equivalent replacement, and improvement made within the spirit and principle of the present invention should be included in the protection scope of the present invention.
Claims (10)
1. A laboratory data management method, comprising:
acquiring current submission application data;
when the current submission application data passes the verification, determining a sample identifier of the current submission sample;
determining the detection plan data of the current submission sample according to the current submission application data and laboratory detection project management data;
and acquiring detection associated data of the current sample to be detected according to the detection plan data, and performing data association storage on the detection associated data and the sample identification.
2. The method of claim 1, wherein determining the test plan data for the current submission sample based on the current submission application data and laboratory test project management data comprises:
determining the detection arrangement time and the detection equipment data of the historical unprocessed submission samples matched with the historical unprocessed submission application data according to the laboratory detection project management data;
and determining the detection plan data of the current submission sample according to the detection scheduling time and the detection equipment data of the historical unprocessed submission sample.
3. The method of claim 2, further comprising, prior to determining a scheduled time for testing of a historical unprocessed submission sample that matches the historical unprocessed submission application data and testing device data based on the laboratory test item management data:
acquiring detection standard updating data, equipment identification data and the historical unprocessed submission application data;
and determining the laboratory detection project management data according to the detection standard updating data, the equipment identification data and the historical unprocessed submission application data.
4. The method according to claim 1, wherein obtaining detection-related data of the current submission sample according to the detection plan data, and storing the detection-related data in data association with the sample identifier, comprises:
acquiring detection result data according to the detection plan data;
performing at least one audit on the detection result data to obtain audit record data;
and performing data association storage on the detection result data, the audit record data and the sample identifier.
5. The method of claim 4, further comprising, after storing the detection correlation data in data correlation with the sample identification:
when the examination result data passes the examination, generating an initial examination report according to the examination result data;
and editing the initial detection report according to the report language support type to generate a target detection report, and sending the target detection report to a target user.
6. The method of claim 5, further comprising, after sending the target detection report to a target user:
acquiring feedback data of the target user to the target detection report;
when the feedback data are abnormal feedback data, obtaining detection process tracing data;
and sending the detection process tracing data to the target user.
7. The method of claim 5, further comprising, after storing the detection correlation data in data correlation with the sample identification:
acquiring sampling recovery sample data;
and performing data association storage on the sampling recovery sample data and the sample identification, and sending the sampling recovery sample data to the target user.
8. A laboratory data management apparatus, comprising:
the data acquisition module is used for acquiring current submission application data;
the sample identification determining module is used for determining the sample identification of the current submission sample when the current submission application data passes the auditing;
the detection plan data determining module is used for determining the detection plan data of the current submission sample according to the current submission application data and the laboratory detection project management data;
and the data association storage module is used for acquiring the detection association data of the current submission sample according to the detection plan data and performing data association storage on the detection association data and the sample identifier.
9. An electronic device, characterized in that the electronic device comprises:
at least one processor; and
a memory communicatively coupled to the at least one processor; wherein the content of the first and second substances,
the memory stores a computer program executable by the at least one processor to enable the at least one processor to perform the laboratory data management method of any one of claims 1-7.
10. A computer-readable storage medium, having stored thereon computer instructions for causing a processor, when executed, to implement the laboratory data management method of any one of claims 1-7.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202210891089.XA CN115187125A (en) | 2022-07-27 | 2022-07-27 | Laboratory data management method, device, equipment and medium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202210891089.XA CN115187125A (en) | 2022-07-27 | 2022-07-27 | Laboratory data management method, device, equipment and medium |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN115187125A true CN115187125A (en) | 2022-10-14 |
Family
ID=83521723
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202210891089.XA Pending CN115187125A (en) | 2022-07-27 | 2022-07-27 | Laboratory data management method, device, equipment and medium |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN115187125A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115660018A (en) * | 2022-12-14 | 2023-01-31 | 中化现代农业有限公司 | Data sampling method and device for sample to be checked, electronic equipment and storage medium |
| CN116433162A (en) * | 2023-04-17 | 2023-07-14 | 北京建工环境修复股份有限公司 | Reagent consumable management method, device, electronic equipment and storage medium |
| CN116596197A (en) * | 2023-07-18 | 2023-08-15 | 青岛博什兰物联技术有限公司 | Standard public service platform based on block chain technology |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107644151A (en) * | 2017-09-01 | 2018-01-30 | 东莞博奥木华基因科技有限公司 | A kind of data management-control method and system for genetic test laboratory |
| CN110610095A (en) * | 2019-07-26 | 2019-12-24 | 上海百检网络技术有限公司 | Report traceability method, server and user side |
| CN113192582A (en) * | 2021-05-26 | 2021-07-30 | 长沙迈迪克智能科技有限公司 | Laboratory informatization management method and system and storage medium |
| CN113850534A (en) * | 2021-11-30 | 2021-12-28 | 南昌协达科技发展有限公司 | Plan management method, system, readable storage medium and computer device |
| CN114155930A (en) * | 2021-11-26 | 2022-03-08 | 广州金域医学检验中心有限公司 | Report issuing method, device, equipment and storage medium |
-
2022
- 2022-07-27 CN CN202210891089.XA patent/CN115187125A/en active Pending
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107644151A (en) * | 2017-09-01 | 2018-01-30 | 东莞博奥木华基因科技有限公司 | A kind of data management-control method and system for genetic test laboratory |
| CN110610095A (en) * | 2019-07-26 | 2019-12-24 | 上海百检网络技术有限公司 | Report traceability method, server and user side |
| CN113192582A (en) * | 2021-05-26 | 2021-07-30 | 长沙迈迪克智能科技有限公司 | Laboratory informatization management method and system and storage medium |
| CN114155930A (en) * | 2021-11-26 | 2022-03-08 | 广州金域医学检验中心有限公司 | Report issuing method, device, equipment and storage medium |
| CN113850534A (en) * | 2021-11-30 | 2021-12-28 | 南昌协达科技发展有限公司 | Plan management method, system, readable storage medium and computer device |
Non-Patent Citations (1)
| Title |
|---|
| 陈晓佳: "实验室信息管理系统的设计与实现", 《中国优秀硕士学位论文全文数据库信息科技辑》, pages 1 - 79 * |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115660018A (en) * | 2022-12-14 | 2023-01-31 | 中化现代农业有限公司 | Data sampling method and device for sample to be checked, electronic equipment and storage medium |
| CN116433162A (en) * | 2023-04-17 | 2023-07-14 | 北京建工环境修复股份有限公司 | Reagent consumable management method, device, electronic equipment and storage medium |
| CN116596197A (en) * | 2023-07-18 | 2023-08-15 | 青岛博什兰物联技术有限公司 | Standard public service platform based on block chain technology |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN115187125A (en) | Laboratory data management method, device, equipment and medium | |
| Harter et al. | Does software process improvement reduce the severity of defects? A longitudinal field study | |
| US20040088324A1 (en) | System providing receipt inspection reporting | |
| CN107844875A (en) | Green product management system and method | |
| CN111461517A (en) | Intelligent information system for planning laboratory workflow | |
| CN111667252A (en) | Enterprise risk management and control platform system | |
| CN115185888A (en) | Enterprise environment-friendly archive management method, device, equipment and storage medium | |
| Dhanalaxmi et al. | A fault prediction approach based on the probabilistic model for improvising software inspection | |
| CN116245410A (en) | Inspection and detection reporting system and method for oil and gas storage and transportation equipment | |
| TWI284846B (en) | Semiconductor automation system for a daily check and method thereof | |
| CN109840642B (en) | Engineering site laboratory supervision system | |
| Bekher et al. | Automation of control processes in the non-destructive testing units | |
| Freeman et al. | Introduction to ISO 15189: a blueprint for quality systems in veterinary laboratories | |
| CN111047274B (en) | Engineering design drawing examination method and system | |
| JP4268168B2 (en) | Inspection management system, inspection management apparatus, and inspection management method | |
| English | Total quality data management (TQdM) | |
| CN113051165A (en) | Method, device, monitoring server and medium for processing test order | |
| JP2011113217A (en) | Reliability analysis device and method | |
| Iqbal et al. | Forward Engineering Completeness for Software by Using Requirements Validation Framework (S). | |
| Adams et al. | Ethics Training Is Essential for Environmental Laboratories | |
| CN108256805B (en) | Method and device for realizing electronic pair order of oil import business | |
| Wang | Design and implementation of a process control system for product inspection | |
| Worthington | Two data bases in every garage: Information quality systems | |
| CN116629770A (en) | Supplier data auditing method and system based on graphical identification technology | |
| Lee et al. | On the Performance Management System to Analyse the Effectiveness of Type Approval System for Railway Vehicle |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination |