How time flies! It always goes by inadvertently. Achievements belong to the past. A new round of work is coming. Let's act at once and write a plan. So do you really know how to write a good plan? The following are five inspection work plans that I have compiled for you. Welcome to read the collection.
Inspection work plan 1 1. Improve service quality and strengthen clinical communication.
1, coordinate with the medical department, organize a joint meeting between the clinical department and the clinical department, and * * * negotiate to solve the problems in their work.
2, solicit opinions and suggestions from relevant departments on the clinical laboratory, in order to improve the clinical laboratory work.
3. Regularly hold a briefing on the inspection items in the clinical laboratory to publicize the significance of the inspection items carried out by the clinical laboratory, so that the inspection items carried out by the clinical laboratory can be closely combined with clinical diagnosis and treatment.
Second, strengthen communication with hospital leaders and win the support of all parties.
1, strive for the understanding and support of hospital leaders, and introduce 2-3 professionals to make up for the shortage of department personnel. Realize rational division of labor and scientific development.
2. If conditions permit, try to buy:
Chemiluminescence immunoassay analyzer 1 set (about 90,000 yuan) can improve the accuracy of existing detection items, increase experimental detection items, and provide more and more diagnostic detection items for clinic.
Automatic bacterial identification instrument 1 set (about 300,000 yuan) can improve the accuracy and timeliness of bacterial identification, and advance the work of bacterial identification from the current 3 days to 8- 12 hours.
1 digital microscope (about 20-30 thousand yuan) can improve the objectivity and accuracy of morphological experimental diagnosis.
3. Strive to send 1 personnel to higher-level hospitals for further study every year.
Third, promote the harmony between doctors and patients and improve the management level of departments.
1, improve the detail management within the department, so that every rule and regulation of the department can be implemented and run through every link of the department's work.
2. Optimize the process of taking report forms from outpatients, so that patients can spend the least time, run the least distance and get the most timely inspection report.
3, the implementation of window smile service, let patients feel warm from the spirit, reduce psychological pressure.
20xx is a brand-new year. With the pilot reform of public hospitals, all inspectors are willing to make their own efforts and contributions to the pilot reform of hospitals. Let laboratory work take advantage of the new medical reform, by going up one flight of stairs!
First, the business of the department is growing, and the department is being systematically built. In the case of constantly saturated workload, it is necessary to introduce excellent professional and technical personnel.
Second, the clinical blood consumption has increased significantly. In order to facilitate patients and improve the inspection institutions, blood from blood banks should be used as soon as possible.
Three, in order to meet the requirements of secondary hospitals in 2009, to meet the evaluation standards, next year will send professional and technical personnel to study indoor quality control, and intends to participate in the inter-laboratory quality evaluation plan organized by the Clinical Laboratory Center of the Ministry of Health.
Fourth, the annual business income of inspection items increased, especially for most cytological tests. Next year, it is planned to establish a pathological room for cytological examination, and clinicians with professional doctor certificates must be sent for further study.
Five, strengthen learning, through practice, and strive to publish two provincial papers.
This year is a very important and special year for us. If Chinese medicine hospital is like a dragon, after overcoming difficulties and hardships, it is fully prepared before the dragon takes off. This year is a full year, fruitful and even more brilliant next year.
Inspection work plan 2 1. Convene a conference on health supervision in the whole city. Summarize last year's work, discuss the development of disease control and inspection ability, talent introduction and technical personnel training, and commend the advanced collectives and individuals of county (city) quality control assessment last year.
Two, do a good job in emergency inspection of infectious diseases and public health emergencies. Do a good job in the material reserve for emergency inspection, and provide scientific data and technical support for ensuring the timely disposal of public health emergencies.
The third is to hold the annual meeting of the city's AIDS screening laboratories, summarize the quality evaluation work of AIDS screening laboratories last year, issue certificates to the excellent laboratories, and put forward requirements for the next step.
Four, accept and complete the qualification supervision and evaluation of the Provincial Bureau of technical supervision.
Five, held the city's health inspection quality control meeting, arrange the annual quality control tasks.
Six, the construction of digital laboratory information management system was officially put into operation.
Seven, held in the county (city) district health inspection professional and technical training courses.
Eight, the county (city) district rural drinking water safety engineering construction and testing for comprehensive supervision.
Nine, the use of existing instruments and equipment to carry out the detection of sodium benzoate, potassium sorbate, saccharin sodium and other items in food.
Ten, according to the deployment of the province, undertake and complete the food safety risk monitoring and sampling inspection and testing work of the Provincial Food and Drug Administration.
Eleven, earnestly complete the national and provincial arrangements for all kinds of quality control assessment. Twelve, strengthen the construction of laboratory hardware, and carry out the determination of mercury in food, water quality and cosmetics after the planned atomic fluorescence spectrometer is in place; Vigorously cultivate and introduce professional talents, and increase 2-3 professional and technical personnel through social recruitment.
Thirteen, strengthen the horizontal contact in business, learn from each other's strong points, and comprehensively improve the technical level of testing and inspection. It is planned to conduct technical exchanges with the Municipal Environmental Monitoring Station, the Central Plains Water Testing Center and the Animal Products Testing Institute of the Municipal Animal Husbandry Bureau to exchange needed goods, and some instruments will share resources.
Fourteen, complete the temporary mandatory work
Inspection Work Plan Part 3 Incoming Inspection Specification
1, use
Ensure the quality of purchased materials and external processing materials meet the specified requirements.
2. Scope
It is suitable for the inspection and test of all raw materials, external processing ingredients, auxiliary materials, packaging materials and other outsourced materials.
3. Responsibility
① The Quality Department is responsible for compiling (incoming inspection instruction).
The warehouse keeper is responsible for registering foreign materials and notifying the incoming inspector.
(3) Incoming inspectors are responsible for the inspection and test of incoming materials and the release of materials.
4. Definition
① Qualified products: materials or products that meet the specified specifications, standards and functional requirements. ② Non-conforming products: materials or products that do not meet the specified specifications and functional requirements. 5.a. Inspection-free materials:
① The Quality Department establishes (inspection-free list) for materials that our factory does not have inspection conditions or have little impact on products ② When inspection-free items enter the factory, the supplier is required to attach the factory inspection certificate as the inspection-free materials specified in the certificate (inspection-free material list) for trial production. When the test fails, it should be recovered in time and the products produced should be inspected comprehensively. According to the specific (nonconforming product planning) for processing. B. Inspection contents:
① When the supplier delivers the goods, the materials will be placed in the area to be inspected, and the warehouse keeper will check the contents and notify the incoming inspection.
Members to check. After receiving the notice, the incoming inspection personnel shall conduct sampling inspection according to the drawings and relevant samples. If it is judged as qualified, it has just been stamped with the blue incoming inspection seal. Warehouse personnel put in the warehouse, put unqualified labels on those judged unqualified, put them in the unqualified area, and fill in the incoming inspection report in time after inspection.
(2) When any abnormality is found in the incoming inspection, the incoming inspector shall immediately fill in the Incoming Inspection Report and submit it together with the unqualified samples to the Minister of Quality Department for confirmation. The disposal of unqualified incoming materials shall be carried out according to (nonconforming product procedure). When the supplier's incoming materials are seriously unqualified, the incoming inspection personnel should fill in (corrective and preventive measures procedure report) and send it to the supplier, asking them to report the improvement measures.
(3) The quality department clerk takes the monthly feed quality status (supplier quality evaluation form) as the evaluation data of suppliers, and sends a copy to the purchasing department.
Process inspection specification
1, use
In order to effectively control the quality of the production process and prevent unqualified products from producing and flowing into the next process.
2. Scope of application
It is suitable for the process inspection of process products in our factory.
3. Responsibility
① This procedure is formulated and implemented by the Quality Department with the cooperation of relevant departments.
② The workshop director of the production department and IPQC are responsible for the "first inspection" confirmation of each process.
③ The director of quality department is responsible for reviewing the inspection report of IPQC and tracking the quality status.
4. Definition
① First inspection: refers to the inspection of the first part of each working procedure, the change of operating conditions or the change of product specifications.
Inspection of the first product in mass production.
② Self-inspection: The operator checked the products produced by himself, and there was no record.
(3) Inspection: Check back and forth whether all important stations and types of work are carried out according to specifications and standards.
④ Full inspection: conduct a comprehensive inspection of a product standard in the production process.
⑤ Spot check: Spot check and test the important dimensions, functions and performance strength of the product to ensure that the product quality reaches the standard at all stages.
5, inspection standard operation content
① Process inspection is based on samples, drawings and work instructions (product inspection specifications) as the standard for quality judgment.
② First article inspection:
The person in charge of the production workshop and IPQC inspect the first part of the process product, and inspect and inspect the parts that need to be assembled or matched according to the dimensions in the engineering specification. After passing the inspection, the leader of IPQC will sign the first sample, and IPQC must fill in the first inspection record. When the first product is confirmed to be qualified, the production workshop can mass produce it.
(3) patrol inspection:
IPQC conducts inspection according to relevant (inspection specifications) samples and other materials. A certain number of products are randomly selected for inspection at a time. After the inspection is completed, IPQC fills in the relevant inspection report. IPQC team leader or product
The director of quality department is responsible for the audit.
(4) semi-finished products spot check:
IPQC conducts sampling inspection on semi-finished products produced in the process according to relevant (product specifications) samples and other materials, fills in relevant reports, and submits them to the Minister of Quality Department and the relevant QC team leader for review and confirmation.
(5) Inspection rules for semi-finished products with sequential changes:
A. The semi-finished products with process change shall be supervised by IPQC, and the semi-finished products with process change shall be marked with IPQC and stamped with qualified marks. When the semi-finished products fail to pass the inspection, they should be labeled with red unqualified marks.
B, the person in charge of each process, IPQC, must inspect the incoming materials of the previous process, and return the unqualified materials.
Go back to the previous procedure and conduct a comprehensive inspection.
⑥ Disposal of nonconforming products:
Return inspection: The unqualified semi-finished products shall be handled according to (Nonconforming Product Management Procedure). All landowners record report:
IPQC must count the qualified rate of relevant process quality in the above-mentioned relevant inspection records. The quality department clerk will count and file the workshop quality for each IPQC report every month.
Outbound inspection specification
1, use
Ensure that the finished products are inspected according to relevant regulations before leaving the factory or delivery. And meet customer requirements to prevent defective products from flowing to customers.
2. Scope of application
Applicable to the final inspection of all products produced by our factory.
3. Responsibility
A. Quality Department: responsible for compiling the delivery inspection instruction.
B. Quality Department: OQC is responsible for delivery inspection.
C production department: responsible for the processing and inspection of finished products and the rework of defective products.
4, homework content
A. The packaged finished products completed by the workshop of the production department will be sent to the area for inspection and labeling, and delivered by the production department.
Fill in (finished product inspection notice) occasionally and inform OQC of quality department for inspection.
B, OQC inspectors produce according to samples, engineering specifications, customer requirements and finished product inspection specifications.
For single sample inspection, record the results on (finished product inspection report) and submit them to the director of quality department for approval. If the products pass the inspection, the qualified mark shall be affixed on the finished product mark, and the production workshop shall be informed. Qualified finished products should be moved to the qualified area in time, or hung with qualified signs.
C. If the inspection is unqualified, OQC shall submit the unqualified samples together with the inspection report of unqualified finished products.
Submit it to the Quality Department for review and confirmation. The person in charge of the quality department should sign the treatment results on the (finished product inspection report) and fill in the (corrective and preventive measures report), and then inform the production department and the sales department to put the unqualified finished products into the unqualified finished product area or hang the unqualified sign.
D, responsible workshop after receiving the unqualified finished product inspection report, to arrange personnel according to (corrective and preventive measures.
Report) for rework, and the selected defective products shall be handled according to (nonconforming product management procedure).
E. The reworked finished products can only be put into storage and shipped after being rechecked by OQC.
F, quality department clerk should statistics monthly qualified rate of finished products, and make relevant reports, as the relevant basis for quality problem analysis and improvement.
In 20xx, with the correct guidance and support of hospital leaders and the full cooperation of all departments, Qi Xin, a comrade in the clinical laboratory, worked together to establish a high sense of professionalism and responsibility, took the initiative to emancipate his mind, updated his ideas, worked hard around the hospital center, and combined with the characteristics of the department's work, constantly improved the medical quality, ensured medical safety and improved the quality of general medical care, and successfully completed all the work of the department.
Although 20xx has made some achievements, our work is still not detailed and in-depth. In 20xx, the clinical laboratory will cooperate with the hospital reform pilot, effectively improve the service quality, and strictly control the internal management of the department, so as to make the department work to a higher level! 20xx laboratory work plan is as follows:
First, improve service quality and strengthen clinical communication.
1, coordinate with the medical department, organize a joint meeting between the clinical department and the clinical department, and * * * negotiate to solve the problems in their work.
2, solicit opinions and suggestions from relevant departments on the clinical laboratory, in order to improve the work of the clinical laboratory.
3. Hold regular briefings on various inspection items in the clinical laboratory, publicize the significance of the projects carried out by the clinical laboratory, and closely integrate the inspection items carried out by the clinical laboratory with clinical diagnosis and treatment.
Second, strengthen communication with hospital leaders and win the support of all parties.
1, strive for the understanding and support of hospital leaders, and introduce 2-3 professionals to make up for the shortage of department personnel. Realize rational division of labor and scientific development.
2. If conditions permit, try to buy:
Chemiluminescence immunoassay analyzer 1 set (about 90,000 yuan) can improve the accuracy of existing detection items, increase experimental detection items, and provide more and more diagnostic detection items for clinic.
Automatic bacterial identification instrument 1 set (about 300,000 yuan) can improve the accuracy and timeliness of bacterial identification, and advance the work of bacterial identification from the current 3 days to 8- 12 hours.
1 digital microscope (about 20-30 thousand yuan) can improve the objectivity and accuracy of morphological experimental diagnosis.
3. Strive to send 1 personnel to higher-level hospitals for further study every year.
Third, promote the harmony between doctors and patients and improve the management level of departments.
1, improve the detailed management within the department, so that every rule and regulation of the department can be implemented and run through every link of the department's work.
2. Optimize the process of outpatient report, so that patients can spend the least time, run the least distance and get the most timely inspection report.
3, the implementation of window smile service, let patients feel warm from the spirit, reduce psychological pressure.
20xx is a brand-new year that connects the past and the future. With the pilot reform of public hospitals, all inspectors are willing to make their own efforts and contributions to the pilot reform of hospitals. Let the laboratory work take advantage of the new medical reform, by going up one flight of stairs!
Inspection Work Plan 5 20xx Under the supervision and guidance of the superior quality supervision department, we have successfully completed the inspection work throughout the year in strict accordance with the requirements of the Measures for the Supervision and Administration of Motor Vehicle Safety and Technical Inspection Institutions. By reviewing and summarizing the management work of this company this year, the typical problems existing at present are sorted out, providing materials for subsequent improvement. On this basis, we hereby put forward the 20xx annual management work plan as follows:
First, step up the revision of the management system.
The new Administrative Measures for Accreditation of Inspection and Testing Institutions, namely the Order of General Administration of Quality Supervision, Inspection and Quarantine (163), was promulgated and implemented on August 1 day of 20xx. According to the requirement that the management system must be updated by the provincial quality supervision bureau 1, our company plans to complete the management system update process by June next year 1. Due to some changes in the new Administrative Measures for Accreditation of Inspection and Testing Institutions and the original Criteria for Accreditation of Laboratory Qualification, it is planned to change the management system documents to meet all the elements in the Administrative Measures for Accreditation of Inspection and Testing Institutions, and improve the management system to ensure its effective operation.
Second, the inspection equipment update plan
2 186 1-20xx "Items and Methods of Motor Vehicle Safety Technical Inspection" 8. 1/8.2, 20xx March 1 day, requirements for equipment transition period, loading braking method and automatic measuring device. Our company's security workshop plans to install a loading reaction test-bed and an automatic measuring device for external dimensions at 20xx 10. Ensure the continuous improvement of the test equipment used by the company.
Third, continue to attach importance to training and communication.
In order to better implement the 2 186 1-20xx standard, this year, our company actively participated in the publicity and training of the new standard of provincial and municipal quality supervision departments. Through external and internal training, our employees' understanding of the new standards has been significantly improved. In internal training, significant progress has been made in training intensity, training planning and implementation. However, there are also some problems, such as low participation in training and the training effect needs to be improved. According to the existing experience feedback, we will pay more attention to the quality of training next year, not the quantity. Strengthen internal training, fully share the practical gains with you, and pave the way for further improvement of the system. (See 20xx annual training plan for details)
In addition to training, 20xx will pay more attention to communication with various departments in management, improve communication efficiency and promote the integration of management concepts.
Fourth, strengthen the internal management of inspection lines.
In strict accordance with the requirements of the construction and management standards of motor vehicle inspection stations, gradually decompose and compare, clearly understand the preparations, and solve the problems that do not meet the requirements and deficiencies as soon as possible; strict
The requirements of motor vehicle safety performance testing station ensure the safety of on-line vehicles and the authenticity of testing data, and it is absolutely forbidden to carry out on-line testing on vehicles with potential safety hazards and vehicles that do not meet the requirements. In order to ensure the authenticity and accuracy of the safety performance test data of each on-line vehicle and avoid mistakes and bad results caused by negligence, we are responsible for the driving safety of motor vehicles and for every owner who comes to our company for testing.
20xx is a brand-new year that connects the past and the future. In the new year, we should lay a good foundation, improve our business ability, meet new work with excellent testing level, and strive to be the first-class motor vehicle safety performance testing enterprise in the city.
Shijiazhuang hongzhibao automotive vehicle detection co., ltd
Shan Peng Chun
20xx65438+February 15
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