CN110097293A - Laboratory Management System construction method and platform based on relevant criterion file - Google Patents
Laboratory Management System construction method and platform based on relevant criterion file Download PDFInfo
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- G06Q10/00—Administration; Management
- G06Q10/06—Resources, workflows, human or project management; Enterprise or organisation planning; Enterprise or organisation modelling
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- G06Q10/06316—Sequencing of tasks or work
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Abstract
The present invention relates to a kind of Laboratory Management System construction method and platform based on relevant criterion file, belong to the technical field that management is realized from relevant criterion to Laboratory Management System file.Management system process is created, deletes and modified in information management system according to user configuration, it realizes that the job information executed fully according to management system file records, can also increase, delete and modify the node element of each program node in each control program according to user setting.By being docked with quality standard file, normative document certification is decomposed comprehensively enters platform, the System Documents generated are made to meet the requirement of laboratory certification approval, simultaneously, changed by configurable, allow user flexibly, it is simple, efficiently adjust needed for content, solve in the prior art that recording mode is single, treatment effeciency is low, the technical issues of configuration mode is single, is unable to satisfy the requirement of laboratory certification approval.
Description
Technical field
The invention belongs to the technical field of management is realized from relevant criterion to Laboratory Management System file, and in particular to one
Laboratory Management System construction method and platform of the kind based on relevant criterion file.
Background technique
The place that laboratory (Laboratory/Lab) is tested.Laboratory is the cradle of science, is scientific research
Base, the source of development in science and technology plays very important effect to development in science and technology.Either University Scientific Research, production Quality Control, prison
Management or third party's commission are superintended and directed, also or is aerospace, be unable to do without laboratory.In laboratory in use, can generate big
The laboratory information of amount, such as: sample detection information, facility information, instrument and meter information, experimental data, is taken at report information
Expect time, qualification rate etc..
Currently, generalling use in managing laboratory data and being accustomed to write regulation or table according to user
Craft or computer record are carried out, regulation used or table fail to embody the requirement of integral laboratory management system mostly, and record
Mode is single, treatment effeciency is low, and configuration mode is single, is unable to satisfy the requirement of laboratory certification approval.
Summary of the invention
In order to solve the above problems existing in the present technology, the present invention provides a kind of experiments based on relevant criterion file
Room management system construction method and platform, with flexible configuration, efficient process laboratory data and with certification and accreditation standard text
The features such as part is consistent.
Technical solution provided by the invention is as follows:
On the one hand, a kind of Laboratory Management System construction method based on relevant criterion file, comprising:
Management system process is created, deletes and modified in information management system according to user configuration；
The content information of every management system process is set, and the content information information includes workflow, supports
At least one of title, workflow type, support form types, project leader, project grade and project place；
Corresponding Laboratory Management System file is obtained for the management system process, and from the Laboratory Management System
Quality control program quantity is extracted in file and executes standard；
Program quantity and the execution standard are managed according to the quality, establishes control stream for the management system process
Journey, the control process include executing sequence between each quality control program, and the execution standard includes each control journey
The execution content of sequence；
It is wanted according to the node that user setting increases, deletes and modify each program node in each quality control program
Element.
Still optionally further, the Laboratory Management System file is obtained by CMA and/or CNAS review standards of designing, described to be
The management system process obtains corresponding Laboratory Management System file, and extracts from the Laboratory Management System file
Quality manages program quantity and executes standard, further includes: extracts quality from CMA the and/or CNAS review standards of designing and manages journey
Ordinal number amount and execution standard generate System Documents corresponding with quality control program quantity and the execution standard；
The corresponding System Documents include first grade file, second grade file, three levels of files and level Four file；
The first grade file includes quality manual, quality policy, quality objective；
The second grade file includes program file；
The three levels of files include: job instruction, inspection specification or operating instruction；
The level Four file includes: quality record.
Still optionally further, the Laboratory Management System file includes: quality standard file set by user.
Still optionally further, described to increase, delete and modify in each quality control program respectively according to user setting
The node element of a program node, comprising:
User's selection instruction is received, increases and/or delete management selected by the user in default management system process
System process；And/or
It receives user and modifies instruction, display modification interface, so that user modifies Edition Contains.
Still optionally further, further includes:
Preset logical relation is set, when user input and/or selection are consistent co content with the logical relation,
It is automatic to carry out logic selection.
Still optionally further, further includes:
Display logic editing interface, for user setting logical relation；
The logical relation includes: control programmed logic relationship, others' member's authority logic relationship at different levels.
Another aspect, a kind of Laboratory Management System construction platform based on relevant criterion file, comprising:
Project management module, for creating, deleting and modifying management system in information management system according to user configuration
Process, and, for the content information of every management system process to be arranged, the content information information includes workflow
Journey supports title, workflow type, supports in form types, project leader, project grade and project place extremely
It is one few；
Normative document management module, for obtaining corresponding Laboratory Management System file for the management system process,
And extract quality control program quantity from the Laboratory Management System file and execute standard, to control program management module
Send the quality control program quantity and the execution standard；
Program management module is managed, program quantity and the execution standard are managed according to the quality, is the management body
It is that process establishes control process, the control process includes the sequence that executes between each quality control program, described to execute mark
Standard includes the execution content of each control program；
Flow nodes management module increases, deletes and modifies according to user setting and is each in each quality control program
The node element of a program node.
Still optionally further, the control program management module is also used to: receiving user to the logical relation of specific field
Setting shows the specific field according to logical relation set by user output.
Still optionally further, the control program management module is also used to, display logic editing interface, for user setting
Logical relation, the logical relation include quality control programmed logic relationship and others' member's authority logic relationship at different levels, described to patrol
Collect the edition interface that editing interface has the specific field.
Still optionally further, further includes:
Information acquisition module, for receiving each node element value of user's input, setting, and the data that will acquire are to record
Document creation module is sent；
The recording documents generation module, the data for being obtained according to the information acquisition module generate recording documents.
A kind of Laboratory Management System construction method and platform based on relevant criterion file provided in an embodiment of the present invention,
Management system process is created, deleted and modified in information management system according to user configuration, every management system process is set
Content information, content information information include workflow, support title, workflow type, support form types, item
At least one of mesh responsible person, project grade and project place obtain corresponding laboratory room managing body for management system process
It is file, and extracts quality control program quantity from Laboratory Management System file and execute standard, journey is managed according to quality
Ordinal number amount and execution standard establish control process for management system process, and control process includes that each quality is managed between program
Execute sequence, execution standard includes the execution content of each control program, is increased according to user setting, is deleted and modification is each
Quality manages the node element of each program node in program.By being docked with quality standard file, so that body generated
Be the requirement that file meets laboratory certification approval, meanwhile, changed by configurable, allow user flexibly, it is simple, efficiently
Content needed for adjusting, solves in the prior art that recording mode is single, treatment effeciency is low, and configuration mode is single, is unable to satisfy reality
The technical issues of testing the requirement of room certification and accreditation.According to different laboratory room managing demands, system configuration is freely realized, so that with
Family experience is more happy dripping, and " software developer not can be appreciated that the pain of cutting one's body of laboratory practitioner, while laboratory for solution
The pain of cutting one's body of practitioner cannot be expressed in software design " technical problem.
Detailed description of the invention
In order to more clearly explain the embodiment of the invention or the technical proposal in the existing technology, to embodiment or will show below
There is attached drawing needed in technical description to be briefly described, it should be apparent that, the accompanying drawings in the following description is only this
Some embodiments of invention for those of ordinary skill in the art without creative efforts, can be with
It obtains other drawings based on these drawings.
Fig. 1 is a kind of Laboratory Management System construction method stream based on relevant criterion file provided in an embodiment of the present invention
Journey schematic diagram；
Fig. 2 is a kind of Laboratory Management System construction platform based on relevant criterion file provided in an embodiment of the present invention
Structural schematic diagram.
Appended drawing reference: 21- project management module；22- normative document management module；23- manages program management module；24-
Flow nodes management module.
Specific embodiment
To make the object, technical solutions and advantages of the present invention clearer, technical solution of the present invention will be carried out below
Detailed description.Obviously, described embodiments are only a part of the embodiments of the present invention, instead of all the embodiments.Base
Embodiment in the present invention, those of ordinary skill in the art are obtained all without making creative work
Other embodiment belongs to the range that the present invention is protected.
In order to clearly illustrate that the process and advantage of the present embodiment inventive method, the present invention provide a kind of based on correlation
The Laboratory Management System construction method of normative document, the method for the embodiment may include:
Management system process is created, deletes and modified in information management system according to user configuration；
The content information of every management system process is set, content information information include workflow, support title,
At least one of workflow type, support form types, project leader, project grade and project place；
Corresponding Laboratory Management System file is obtained for management system process, and is mentioned from Laboratory Management System file
Take quality control program quantity and execution standard；
Program quantity is managed according to quality and executes standard, is established control process for management system process, is managed process packet
The sequence that executes between each quality control program is included, execution standard includes the execution content of each control program；
Increase, delete and modify the node element of each program node in each quality control program according to user setting.
A kind of Laboratory Management System construction method based on relevant criterion file provided in an embodiment of the present invention, by with
The docking of quality standard file, so that System Documents generated meet the requirement of laboratory certification approval, meanwhile, by that can match
Displacement, allow user flexibly, it is simple, efficiently adjust needed for content, solve that recording mode in the prior art is single, place
The technical issues of reason low efficiency, configuration mode is single, is unable to satisfy the requirement of laboratory certification approval.
Based on a kind of above-mentioned Laboratory Management System construction method based on relevant criterion file, the embodiment of the present invention is provided
One alternative embodiment: Fig. 1 is a kind of Laboratory Management System building based on relevant criterion file provided in an embodiment of the present invention
Method flow schematic diagram, referring to Fig. 1, the Laboratory Management System construction method based on relevant criterion file of the present embodiment can be with
The following steps are included:
S11, management system process is created, deletes and modified in information management system according to user configuration.
The present embodiment is suitable for any quality based on standard criterion file, the item objects of flow management and control, project pair
Professional technique as can be enterprise is managed, and such as can be the control to certain Intellectual Property Right of Enterprises management, and item objects can also be with
It is to be managed to the traffic-operating period of certain business unit's entity, such as managed to the quality of certain disease prevention and control center.
For each item objects, one is created in the Laboratory Management System construction platform based on relevant criterion file
Item record, entrance of the every item record as an item objects, the management of respective item object is entered by the entrance
Sub-platform, in item objects management sub-platform can various files relevant to the item objects, process be managed.
Specifically, the setting carried out according to user, is operated in information management system, is created, deletes and is modified
Item record, item record are management system process.
For example, in a laboratory, in order to carry out project control to laboratory information, using the present embodiment based on base
In the Laboratory Management System construction method of relevant criterion file, in management system construction platform, according to the setting of user,
The creation, deletion and modification of system process are managed in information management system.The system construction platform according to laboratory etc.
Grade and demand, self information management system has the management system process routinely set, in a specific laboratory, according to
User demand edits management system process in information management system.
S12, the content information that every management system process is arranged, content information information include workflow, support table
At least one of title, workflow type, support form types, project leader, project grade and project place.
Specifically, the content information of every management system process is settable, and content information may include one of the following
Or it is multiple: workflow, support title, workflow type, support form types, project leader, project grade and
Project place.
For example, user can setting be every according to their own needs in system construction platform in laboratory calibration
Workflow, the project information for supporting table, such as the setting entitled reagent of project are received, and project grade is level Four, project
Place is the laboratory A, and project leader is that receive people small red etc..It is worth noting that user can be according to self-demand to project
The project information of record is modified and is set, and is only enumerated herein, is not to limit.
S13, corresponding Laboratory Management System file is obtained for management system process, and from Laboratory Management System file
Middle extraction quality control program quantity and execution standard；
S14, program quantity is managed according to quality and executes standard, establish control process, control stream for management system process
Journey includes the sequence that executes between each quality control program, and execution standard includes the execution content of each control program.
Specifically, in the workflow of management system process, support table generate, corresponding normative document is obtained,
Control program number amount is extracted in normative document and executes standard, according to control process quantity and is executed standard, is established corresponding pipe
Flow control journey generates corresponding item record with this.Wherein, control process may include that the execution between each control program is suitable
Sequence, execution standard may include the execution content of each control program.
For example, according to laboratory own tier and classification, choosing corresponding laboratory in lab management information processing
Normative document, and extract control program number amount from laboratory standard file and execute standard, according to the control program extracted
It quantity and executes standard and establishes corresponding control process, control process includes executing sequence between each control program, executes mark
Standard includes the execution content of each control program, generates corresponding workflow with this, supports table.
Further, normative document can be the standard of the formulations such as country, employer's organization, and Laboratory Management System file can
It, can also be by the matter of user's sets itself such as CMA and/or CNAS review standards of designing to be obtained by CMA and/or CNAS review standards of designing
Measure normative document.Wherein, CNAS is China National Accreditation Service for Conformity
The abbreviation of Assessment is the regulation according to " People's Republic of China's certification and accreditation regulations ", is approved by national authentication and supervised
Administration committee ratifies the authorized by state mechanism for setting up and authorizing, unified to be responsible for certification authority, laboratory and inspection body etc.
The approval work of associated mechanisms.CMA is the contracting of China Metrology Accreditation (china metrology Accreditation/approval)
It writes.Obtain laboratory qualification certification (measurement certification) certificate of competency testing agency, can by the project for ratifying to list on certificate,
Indicated on detection (detection, test) certificate and report using CMA.
For example, meet CMA and/or CNAS Valuation Standard to promote the standardization level of laboratory information process flow,
It can import system construction platform using CMA and/or CNAS review standards of designing as normative document in the present embodiment and store, and according to
CMA and/or CNAS review standards of designing therefrom extracts control program number amount and executes standard, generates and control program quantity and execution
The corresponding System Documents of standard.Standard accreditation criteria is country or the publication of standard evaluation committee.
During carrying out CMA and/or CNAS review standards of designing, the system construction platform of the present embodiment realizes entirely for the first time
The information solutions that CMA and/or CNAS certification enters platform are decomposed in face, automatically obtain certification.By taking ISO9001 as an example, according to
The system requirement in laboratory, analyzes ISO9001 standard, and user and/or platform carry out it to decompose conversion, the system of generation comprehensively
File includes level Four file.Wherein, first grade file includes quality manual, quality policy, quality objective；Second grade file is program text
Part, it is necessary to which contain 6 program files required by 9001: document control, record control, internal check, rejected product are controlled, entangled
Positive measure, precautionary measures；Three levels of files are supportive file or management system etc, including job instruction, inspection procedure, pipe
Reason method, management system etc.；Level Four file is quality table.According to standard, setting includes the content in above-mentioned level Four file.Root
Normative documents at different levels according to the standard for importeding into system construction platform, in land identification ISO9001 standard.If ISO14001 body
System, first grade file is then environment handbook；If it is ISO18001 system, level-one is occupation healthy security management handbook.User can
The selection of standard is carried out according to the different systems in laboratory, herein without limitation.
For example, 4.4 require " to have and be engaged in inspection in national standard " examining testing agency's qualification certification accreditation criteria "
Detection device facility necessary to detection activity " completes certification and accreditation to reach national requirements, and enterprise needs to mark country
Standard is converted.In the present embodiment, the conversion method of System Documents are as follows: first according to national standard, generate level-one text
Part --- quality manual, quality manual require to correspond with the accreditation criteria of national requirements, and country 4.4 requires " to have and be engaged in
Examine detection device facility necessary to detection activity ", enterprise-quality handbook correspondingly, " has and is engaged in complete target
Examine detection device facility necessary to detection activity ", Section four of chapter 4 is set up, theme are as follows: installations and facilities, short title
QA is required corresponding with country 4.4.Secondly, first grade file is directed toward second grade file, second grade file is further refined, QB " the equipment phase
Between verification procedures ", in second grade file, be directed toward three levels of files.Three levels of files QC " electronic analytical balance working specification ", in three-level
In file, it is directed toward level Four file.Level Four file is record form, and QD " is examined and verified registration form during detecting instrument ".
In the system construction platform of the present embodiment, control program can be workflow, workflow and second level text
Program file in part corresponds to each other, and so on corresponded to, CMA and/or CNAS Valuation Standard is decomposed comprehensively, is shown in
In platform.For example, extracting workflow step number according to System Documents standard and executing workflow criteria.According to what is extracted
Workflow step number and execution workflow criteria establish corresponding control process for the item record, and control process includes
Sequence is executed between each workflow step, execution workflow criteria includes that the execution of each workflow step is suitable
Sequence.
Further, normative document further includes quality standard file set by user.The experiment approved for national authentication
Room can choose national standard when carrying out normative document selection；National authentication accredited laboratory is not obtained for some,
When carrying out normative document selection, the quality standard system file of user oneself setting may be selected.
S15, it is wanted according to the node that user setting increases, deletes and modify each program node in each quality control program
Element.
Specifically, the node element of each program node in each control program can be carried out according to the setting of user
Increase, delete and modifies.It specifically includes: receiving user's selection instruction, increase in default management system process and/or delete and use
Management system process selected by family；And/or it receives user and modifies instruction, display modification interface, so that user modifies content
Editor.
For example, the management system construction platform of the present embodiment receives this work in reagent in laboratory calibration
It under project, instructs according to the user's choice, drags preset " time " element, increase this newly now.It can also be according to user
Selection instruction, drag preset " time " element and deleted.It can also increase option newly according to user instruction, be compiled
Volume, increase " receiving people " element, realizes that the configurable of information changes.It is worth noting that the present embodiment is only changed configurable
It enumerates, is not to limit.
Further, in the Laboratory Management System construction method based on normative document of the present embodiment, further includes: setting
Preset logical relation, it is automatic to carry out logic selection when user's input and/or selection are consistent co content with logical relation.
For example, the examination & approval logic of approving person is preset in laboratory calibration, it is defeated in the operator of different stage
When entering and/or selecting copending content, the corresponding approval process of Auto-matching.It is worth noting that being herein pre- to logic
If enumerate, it is any realize logic judgment method, belong to protection scope of the present invention.
For the ease of user's operation, present invention method further include: display logic editing interface, for user setting
Logical relation；Logical relation includes: control programmed logic relationship, others' member's authority logic relationship at different levels.
For example, user can carry out logical edit according to demand, equally by taking examination & approval as an example, user can set according to self-demand
Permission is consulted in approving person and examination & approval.Only logical edit is enumerated herein, is not to limit.
A kind of Laboratory Management System construction method based on relevant criterion file provided in an embodiment of the present invention, according to
Family configuration creates in information management system, deletes and modifies management system process, and the content of every management system process is arranged
Information, content information information include workflow, support title, workflow type, form types, project is supported to be responsible for
At least one of people, project grade and project place obtain corresponding Laboratory Management System file for management system process,
And from Laboratory Management System file extract quality control program quantity and execute standard, according to quality manage program quantity and
Execution standard establishes control process for management system process, and control process includes that the execution between each quality control program is suitable
Sequence, execution standard include the execution content of each control program, increase, delete and modify each quality according to user setting and manage
The node element of each program node in program.By being docked with quality standard file, so that System Documents generated accord with
Close the requirement that laboratory certification is approved, meanwhile, changed by configurable, allow user flexibly, it is simple, efficiently adjust needed for
Content, solves in the prior art that recording mode is single, treatment effeciency is low, and configuration mode is single, is unable to satisfy laboratory certification
The technical issues of requirement of approval.According to different laboratory room managing demands, system configuration is freely realized, so that user experience is more
Add happy dripping, solves that " software developer not can be appreciated that the pain of cutting one's body of laboratory practitioner, while laboratory practitioner
Pain of cutting one's body cannot be expressed in software design " technical problem.
The above-mentioned Laboratory Management System construction method based on relevant criterion file, the embodiment of the present invention are realized in order to cooperate
A kind of Laboratory Management System construction platform based on relevant criterion file is provided.Fig. 2 is one kind provided in an embodiment of the present invention
The structural schematic diagram of Laboratory Management System construction platform based on relevant criterion file.Referring to fig. 2, the present embodiment based on phase
Close the structure of the Laboratory Management System construction platform of normative document, comprising: project management module, 21, normative document management mould
Block 22, control program management module 23, flow nodes management module 24.
Project management module 21, for creating, deleting and modifying management body in information management system according to user configuration
It is process, and, for the content information of every management system process to be arranged, content information information includes workflow, supports
At least one of title, workflow type, support form types, project leader, project grade and project place；
Normative document management module 22, for obtaining corresponding Laboratory Management System file for management system process, and
Quality control program quantity is extracted from Laboratory Management System file and executes standard, sends matter to control program management module
Buret control program quantity and execution standard；
Program management module 23 is managed, is management system process for managing program quantity according to quality and executing standard
Control process is established, control process includes executing sequence between each quality control program, and execution standard includes each control
The execution content of program；
Flow nodes management module 24, it is each in each control program for being increased according to user setting, deleting and being modified
The node element of program node.
Further, control program management module 23 is also used to:
It receives user to set the logical relation of specific field, exports display designated word according to logical relation set by user
Section.
Further, control program management module 23 is also used to:
Display logic editing interface, for user setting logical relation, logical relation include control programmed logic relationship and
Others' member's authority logic relationships at different levels, logical edit interface have the edition interface of specific field
Further, the Laboratory Management System construction platform based on relevant criterion file of the present embodiment, further includes:
Information acquisition module 25, for receiving each node element value of user's input, setting, and the data that will acquire are to note
Document creation module is recorded to send；
Recording documents generation module 26, the data for being obtained according to information acquisition module generate recording documents.
About the device in above-described embodiment, wherein modules execute the concrete mode of operation in related this method
Embodiment in be described in detail, no detailed explanation will be given here.
A kind of Laboratory Management System construction platform based on relevant criterion file provided in an embodiment of the present invention, according to
Family configuration creates in information management system, deletes and modifies management system process, and the content of every management system process is arranged
Information, content information information include workflow, support title, workflow type, form types, project is supported to be responsible for
At least one of people, project grade and project place obtain corresponding Laboratory Management System file for management system process,
And from Laboratory Management System file extract quality control program quantity and execute standard, according to quality manage program quantity and
Execution standard establishes control process for management system process, and control process includes that the execution between each quality control program is suitable
Sequence, execution standard include the execution content of each control program, increase, delete and modify each quality according to user setting and manage
The node element of each program node in program.By being docked with quality standard file, so that System Documents generated accord with
Close the requirement that laboratory certification is approved, meanwhile, changed by configurable, allow user flexibly, it is simple, efficiently adjust needed for
Content, solves in the prior art that recording mode is single, treatment effeciency is low, and configuration mode is single, is unable to satisfy laboratory certification
The technical issues of requirement of approval.According to different laboratory room managing demands, system configuration is freely realized, so that user experience is more
Add happy dripping, solves that " software developer not can be appreciated that the pain of cutting one's body of laboratory practitioner, while laboratory practitioner
Pain of cutting one's body cannot be expressed in software design " technical problem.
A kind of Laboratory Management System construction platform based on relevant criterion file provided in an embodiment of the present invention, is suitable for
Multiple types laboratory can quickly establish management system in conjunction with user demand, rationally, efficiently carry out the optimization of resource and match
It sets, laboratory is helped easily to realize information system management.It can complete to test room Data Integration, and flexible, easy-to-use, efficient note is provided
Record, control mode reduce time cost, opportunity cost spent by manpower management laboratory.
The above description is merely a specific embodiment, but scope of protection of the present invention is not limited thereto, any
Those familiar with the art in the technical scope disclosed by the present invention, can easily think of the change or the replacement, and should all contain
Lid is within protection scope of the present invention.Therefore, protection scope of the present invention should be based on the protection scope of the described claims.
It is understood that same or similar part can mutually refer in the various embodiments described above, in some embodiments
Unspecified content may refer to the same or similar content in other embodiments.
It should be noted that in the description of the present invention, term " first ", " second " etc. are used for description purposes only, without
It can be interpreted as indication or suggestion relative importance.In addition, in the description of the present invention, unless otherwise indicated, the meaning of " multiple "
Refer at least two.
Any process described otherwise above or method description are construed as in flow chart or herein, and expression includes
It is one or more for realizing specific logical function or process the step of executable instruction code module, segment or portion
Point, and the range of the preferred embodiment of the present invention includes other realization, wherein can not press shown or discussed suitable
Sequence, including according to related function by it is basic simultaneously in the way of or in the opposite order, Lai Zhihang function, this should be of the invention
Embodiment person of ordinary skill in the field understood.
It should be appreciated that each section of the invention can be realized with hardware, software, firmware or their combination.Above-mentioned
In embodiment, multiple steps or method can be with storages in memory and by the software of suitable instruction execution platform execution
Or firmware is realized.It, and in another embodiment, can be under well known in the art for example, if realized with hardware
Any one of column technology or their combination are realized: having a logic gates for realizing logic function to data-signal
Discrete logic, with suitable combinational logic gate circuit specific integrated circuit, programmable gate array (PGA), scene
Programmable gate array (FPGA) etc..
Those skilled in the art are understood that realize all or part of step that above-described embodiment method carries
It suddenly is that relevant hardware can be instructed to complete by program, the program can store in a kind of computer-readable storage medium
In matter, which when being executed, includes the steps that one or a combination set of embodiment of the method.
It, can also be in addition, each functional unit in each embodiment of the present invention can integrate in a processing module
It is that each unit physically exists alone, can also be integrated in two or more units in a module.Above-mentioned integrated mould
Block both can take the form of hardware realization, can also be realized in the form of software function module.The integrated module is such as
Fruit is realized and when sold or used as an independent product in the form of software function module, also can store in a computer
In read/write memory medium.
In the description of this specification, reference term " one embodiment ", " some embodiments ", " example ", " specifically show
The description of example " or " some examples " etc. means specific features, structure, material or spy described in conjunction with this embodiment or example
Point is included at least one embodiment or example of the invention.In the present specification, schematic expression of the above terms are not
Centainly refer to identical embodiment or example.Moreover, particular features, structures, materials, or characteristics described can be any
One or more embodiment or examples in can be combined in any suitable manner.
Although the embodiments of the present invention has been shown and described above, it is to be understood that above-described embodiment is example
Property, it is not considered as limiting the invention, those skilled in the art within the scope of the invention can be to above-mentioned
Embodiment is changed, modifies, replacement and variant.
Claims (10)
1. a kind of Laboratory Management System construction method based on relevant criterion file characterized by comprising
Management system process is created, deletes and modified in information management system according to user configuration；
The content information of every management system process is set, and the content information information includes workflow, supports table
At least one of title, workflow type, support form types, project leader, project grade and project place；
Corresponding Laboratory Management System file is obtained for the management system process, and from the Laboratory Management System file
Middle extraction quality control program quantity and execution standard；
Program quantity and the execution standard are managed according to the quality, establishes control process, institute for the management system process
Stating control process includes the sequence that executes between each quality control program, and the execution standard includes holding for each control program
Row content；
Increase, delete and modify the node element of each program node in each quality control program according to user setting.
2. the project according to claim 1 based on normative document manages system construction method, which is characterized in that the reality
Room management system file is tested to be obtained by CMA and/or CNAS review standards of designing, it is described to be obtained accordingly in fact for the management system process
Room management system file is tested, and extracts quality control program quantity and execution standard from the Laboratory Management System file,
Further include: from CMA the and/or CNAS review standards of designing extract quality control program quantity and execute standard, generate with it is described
Quality manages program quantity and the corresponding System Documents of the execution standard；
The corresponding System Documents include first grade file, second grade file, three levels of files and level Four file；
The first grade file includes quality manual, quality policy, quality objective；
The second grade file includes program file；
The three levels of files include: job instruction, inspection specification or operating instruction；
The level Four file includes: quality record.
3. the project according to claim 1 based on normative document manages system construction method, which is characterized in that the reality
Testing room management system file includes: quality standard file set by user.
4. the project according to claim 1 based on normative document manages system construction method, which is characterized in that described
Increase, delete and modify the node element of each program node in each quality control program according to user setting, comprising:
User's selection instruction is received, increases and/or delete management system selected by the user in default management system process
Process；And/or
It receives user and modifies instruction, display modification interface, so that user modifies Edition Contains.
5. the project according to claim 1 based on normative document manages system construction method, which is characterized in that also wrap
It includes:
Preset logical relation is set, when user input and/or selection are consistent co content with the logical relation, automatically
Carry out logic selection.
6. the project according to claim 5 based on normative document manages system construction method, which is characterized in that also wrap
It includes:
Display logic editing interface, for user setting logical relation；
The logical relation includes: control programmed logic relationship, others' member's authority logic relationship at different levels.
7. a kind of Laboratory Management System construction platform based on relevant criterion file characterized by comprising
Project management module, for management system process to be created, deletes and modified in information management system according to user configuration,
And the content information for every management system process to be arranged, the content information information include workflow, support
At least one of title, workflow type, support form types, project leader, project grade and project place；
Normative document management module, for being the corresponding Laboratory Management System file of management system process acquisition, and from
Quality control program quantity is extracted in the Laboratory Management System file and executes standard, is sent to control program management module
The quality control program quantity and the execution standard；
Program management module is managed, program quantity and the execution standard are managed according to the quality, is the management system stream
Cheng Jianli manages process, and the control process includes executing sequence, the execution standard packet between each quality control program
Include the execution content of each control program；
Flow nodes management module increases, deletes and modifies each journey in each quality control program according to user setting
The node element of sequence node.
8. platform according to claim 7, which is characterized in that the control program management module is also used to: receiving user
Logical relation setting to specific field shows the specific field according to logical relation set by user output.
9. platform according to claim 8, which is characterized in that the control program management module is also used to, display logic
Editing interface, for user setting logical relation, the logical relation include quality control programmed logic relationship and it is at different levels others
Member's authority logic relationship, the logical edit interface have the edition interface of the specific field.
10. platform according to claim 7, which is characterized in that further include:
Information acquisition module, for receiving each node element value of user's input, setting, and the data that will acquire are to recording documents
Generation module is sent；
The recording documents generation module, the data for being obtained according to the information acquisition module generate recording documents.
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| CN113627744A (en) * | 2021-07-21 | 2021-11-09 | 南方医科大学第七附属医院(佛山市南海区第三人民医院) | Community prevention and control information management system, method and storage medium for new major infectious disease |
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| CN114240232A (en) * | 2021-12-25 | 2022-03-25 | 思创数码科技股份有限公司 | Authentication material acquisition method, system, readable storage medium and computer equipment |
| CN117787800A (en) * | 2023-12-29 | 2024-03-29 | 北京中水卓越认证有限公司 | Authentication management system based on engineering construction |
| CN117787800B (en) * | 2023-12-29 | 2024-07-02 | 北京中水卓越认证有限公司 | Authentication management system based on engineering construction |
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