Summary is to review and analyze a certain period, a certain project or certain work afterwards, so as to make regular conclusions. It can make us think, so we need to write a summary Summarize. So do you know how to write a summary? The following is a summary of the pharmaceutical and medical equipment work in 2020 that I compiled. Welcome to read and collect it. Summary of Pharmaceutical and Device Work in 2020 1

In 20xx, under the arrangements of the bureau leaders and with the support of comrades, closely combined with reality, our county’s pharmaceutical and device supervision work comprehensively carried out GSP tracking for pharmaceutical operating enterprises. Certification and re-certification on-site inspection. The standardized pharmacies of county-level medical institutions are re-inspected one by one to ensure the quality of medicines and the safety of medication for the general public. The specific work is now summarized as follows:

1. Standardize approval and strictly control access

Entrusted by the Municipal Bureau to handle the renewal and re-certification of the "Pharmaceutical Business Enterprise License" Data acceptance, on-site acceptance and certification. Junan's legal procedures are strictly reviewed during the acceptance of materials. During the acceptance process, if the acceptance standards are not met, the report will not be reported. If the key conditions are not implemented in practice, the report will not be reported. In 20xx, our bureau cooperated with the Municipal Bureau to inspect and accept 12 pharmaceutical business enterprises for opening, renew and accept 23 certificates, and re-certify 25 companies.

2. Increase efforts and effectively strengthen daily supervision.

In accordance with the spirit of the municipal bureau work meeting at the beginning of the year and combined with the actual situation of the county, a daily supervision and inspection plan for pharmaceutical and device operating enterprises was formulated, and the daily supervision and inspection of pharmaceutical and device operating enterprises and medical institutions were carried out in a planned, targeted and focused manner. Supervision and inspection. Establish a daily work contact system for the company to keep abreast of the company's operating conditions, personnel changes, etc. Throughout the year, 68 pharmaceutical and equipment operating companies were inspected, with key inspection contents:

(1) Renewal, re-certification and changes in license registration items of the "Pharmaceutical Business License" and "GSP Certification Certificate";

(2) Implementation status of the "Good Manufacturing Practice for Pharmaceutical Products" system, materials, and measures;

(3) Operation status of the drug GSP management system of enterprises above the county seat;

(4) Drug purchase channels and qualification review management;

(5) Drug classification and labeling, prescription drug sales management, store appearance, store numbers, etc.;

(6) Drug storage and management status;

(7) On-duty status of quality management personnel;

(8) Check whether there is a rental "Drug Business License" and a rental counter and illegal activities such as operating beyond the scope. Through on-site supervision and inspection of 68 pharmaceutical operating companies in our county, 2 companies failed the on-site acceptance inspection and planned to apply for the withdrawal of their "Pharmaceutical Operating Licenses". Three county-level medical institutions were re-inspected for “standardized pharmacies” and all met the standards for “standardized pharmacies”. This inspection focused on medicines and equipment in the surgical and laboratory departments, and carefully reviewed the qualification certificates and product registration certificates provided by the suppliers. Promote knowledge about adverse event monitoring of drugs and devices.

3. Integrity style

This year, we persisted in being diligent and thrifty, corrected our work attitude, improved our work style, and did not take advantage of work for personal gain or malpractice. At work, we treat people who come to do business with courtesy and serve enthusiastically to avoid the "four difficulties" phenomenon.

IV. Problems

Looking back on the work over the past year, although we have completed various target tasks assigned by the leadership as required, there are still big problems:

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First, the individual work is not professional;

Second, there are no good study habits. 2020 Drug and Device Work Summary 2

1. Progress of key tasks

(1) Establish and improve the drug safety supervision responsibility system and build a safe drug use environment. Establish and improve a drug safety responsibility system in which "local governments bear overall responsibility and regulatory authorities each bear their own responsibilities." Gradually improve the drug safety supervision responsibility system integrating counties, towns, and villages.

Our bureau signed the "20xx Drug Safety Supervision Target Responsibility Letter" with the food and drug supervision offices of each town; it held a drug safety work meeting for drug operating enterprises and relevant health centers to implement the sense of responsibility that "enterprises are the first responsible person". Each supervision office has assigned supervisory responsibilities to department offices, positions, and individuals, and established systems of information officers and coordinators to consolidate responsibilities and realize a drug safety grid-based supervision system with layer-by-layer supervision and layer-by-layer implementation.

(2) Strengthen the supervision of drug circulation and promote the fundamental improvement of the drug circulation market. Since the beginning of this year, we have adopted a working method that combines special inspections with daily supervision and inspections to resolutely investigate and deal with various violations of laws and regulations. We have dispatched 370 drug supervision and law enforcement personnel to supervise and inspect more than 500 drug-related units, focusing on inspections in provinces, Chromium-exceeding capsule products and related illegal advertising products notified by the Municipal Bureau. At the same time, in conjunction with the provincial bureau's "Special Action to Combat Counterfeit and Anti-counterfeit Drugs and Devices" activities, the activities of unlicensed production and distribution of pharmaceutical devices are inspected; the behavior of stealing, passing tickets, and affiliated distribution of pharmaceutical devices; the illegal behavior of distributing pharmaceutical devices beyond the scope and method; illegal storage and transportation of pharmaceutical devices behavior, etc. During the inspection, it was discovered that Chinese medicines were piled everywhere in the warehouse of a health room, and a large number of homemade Chinese medicine preparations were made for sale and use. After the problem was discovered, a case was immediately opened for investigation and the punishment was increased.

Through various measures such as daily supervision, special inspections, and timely orders for rectification when problems are discovered, the drug distribution market in our county has been further standardized, and the industry self-discipline awareness of enterprises has been greatly improved.

1. Carry out health examinations for all pharmaceutical and device practitioners in the county. Establish and improve the health files of units that operate and use pharmaceutical devices, and establish a registration and review system for advertising pharmaceutical devices and non-local enterprises selling pharmaceutical devices in Dali County;

2. Earnestly carry out various special rectification works. Strictly in accordance with national, provincial and municipal requirements, we organized special inspections of chromium-excessing capsule products, organized and convened special meetings of the county's operating enterprises and stock exchanges to implement the special rectification of chromium-excessing capsule products, and issued a notice of accountability for the investigation and punishment of chromium exceeding standards. Supervisory responsibilities; an accountability leading group was established to hold accountable stock exchanges that performed poorly and neglected their duties; special rectification activities were carried out to combat counterfeiting of non-pharmaceuticals and unlicensed distribution of pharmaceutical equipment. Cooperated with the Municipal Inspection Institute to complete the rapid inspection of pharmaceuticals and equipment throughout the year; for non-pharmaceutical products, in labels and instructions, they declare functional indications, indications, or express disease prevention, treatment functions, or medicinal efficacy, as well as the product name and drug Capsule products with the same or similar names and those that fail to obtain inspection reports as required will be suspended from sale, and 6 products including non-drug counterfeit drugs Liuwei Dihuang Pills, Qixuehe Capsules, and Jianweixiaoshi Tablets will be investigated and dealt with; suspected of 9 The company has more than 1,000 boxes of capsule products;

3. Do a good job in collecting corporate integrity data and daily supervision data. Establish and improve supervision and inspection files and corporate integrity files to improve the company's awareness of integrity and self-discipline;

4. Strictly enforce certificate renewal, re-certification and changes. In accordance with the "Weinan City Medical Device Operating Enterprises Acceptance Standards", the proposed acceptance of 4 newly opened pharmacies, the renewal of certificates for 14 medical device operating enterprises; the GSP certification of 9 pharmacies; the change of 3 pharmacies and contact lenses Operator training work.

5. Strengthen the quality supervision of the "three unifications" of essential drugs to improve the distribution rate of essential drugs, and require the "three unifications" distribution companies to expand their warehouses, increase the storage capacity of essential drugs, ensure the supply of essential drugs, and comply with requirements Good warehouse acceptance.

(3) Strengthen the supervision of drug use and promote the further improvement of drug and device management levels in medical institutions.

1. Carry out special rectification of drug and device quality and safety. In accordance with the work arrangements of the county bureau, each institute actively carries out drug and device safety rectification activities in medical institutions within its jurisdiction, actively investigates problematic products, and communicates and coordinates with the county bureau in a timely manner if there are major issues.

2. Strengthen the monitoring of adverse drug reactions, improve the monitoring network, expand the coverage of online reporting units, and improve the quantity and quality of adverse drug reaction reports.

Our bureau and the Health Bureau jointly issued the "Notice on Further Strengthening the Monitoring of Adverse Drug Events" to implement responsibilities, and so far 108 adverse drug reaction reports have been reported.

5. Strengthen the supervision of special drugs, strictly implement the "five specialties" management of special drugs, and ensure the management of special drugs and the safety of medication.

2. Existing problems

1. The foundation of the pharmaceutical industry is relatively weak. The overall scale of the pharmaceutical industry in our county is small, and the overall level of enterprise management is low. 68 urban pharmaceutical operating enterprises implement GSP software system management, but they do not operate normally.

2. The relevant shortcomings of the "Three Unifications" policy and the lack of understanding of pharmaceutical personnel have led to the lagging distribution rate.

III. Work plan

1. Continue to increase market supervision, further standardize the production, operation and use of pharmaceutical devices, and create a safe and reliable medication environment for the people of the county ;

2. Efforts should be made to investigate and deal with key cases, especially those suspected of producing, operating, and using counterfeit drugs and equipment, and we must persist in conducting thorough investigations and getting to the bottom of the matter;

3. Carry out various special inspections in depth, and intensify the supervision and crackdown on unlicensed mobile drug dealers and unlicensed operation of medicines and equipment, especially the crackdown on unlicensed operation and use of medicines and medical equipment in rural areas;

4. Collaborate with industry and commerce, radio and television and other relevant departments to strengthen the supervision of pharmaceutical and device advertising.

5. Strengthen the supervision of participating medical institutions and standardize purchase channels to ensure the implementation of the "three unifications" policy. 2020 Pharmaceutical and Device Work Summary 3

1. The pharmacies of the Department of Medicine and Devices are the windows directly facing patients, serving hundreds of patients every day.

How to facilitate patients, improve service attitude and improve service quality are things that the leaders of our hospital have always been concerned about. We will further strengthen the management of the pharmacy. First of all, strengthen the quality education of personnel. Through a series of measures, such as improving work processes, rationally distributing drugs, and assigning comrades with strong work ability to wait at the window to distribute drugs, etc., we actively mobilize the enthusiasm of employees, work together to overcome difficulties, and strictly follow the standards of the safe pharmacy. And will establish an inspection system for department directors to conduct inspections and supervision of pharmacy work from time to time, solve and correct problems in a timely manner, and actively improve window service attitudes based on actual work conditions, and carry out rational medication guidance, medication consultation and other services.

2. Further strengthen business learning. In 20xx, we will make business learning a top priority. First of all, departments must make reasonable arrangements, stipulate learning content, arrange substitute teachers, and regularly assess learning results. In view of the characteristics of weak foundation and poor basic knowledge, we are going to make the following arrangements: 1. Carry out learning and memorization of the names of the drugs operated by our hospital, conduct regular assessments, and link the assessment results with the creation selection evaluation and the monthly performance salary, or with Individual allocation coefficients are linked to promote learning motivation. 2. Carry out online learning and actively create conditions. The department will use some funds to register for national professional pharmacist tutoring lectures and focus on learning relevant pharmaceutical theories. Through study, everyone's theoretical level has been improved. 3. Actively participate in business studies organized by the hospital. If conditions permit, personnel can be sent to participate in short-term study classes organized by the provincial pharmaceutical association, etc. 4. Increase the learning of new knowledge. Actively carry out the study of clinical medication knowledge such as antibiotic application, clinical rational medication, hormone application management, medication for the elderly, and medication for children. Through learning and updating knowledge, we can cultivate some business backbones and promote the learning of all staff. 5. If conditions permit, one or two comrades with strong professional abilities and good basic knowledge can be sent to participate in clinical pharmacy training courses to promote the development of clinical pharmacy work in our hospital

3. Continue to improve the system and promote department management. In 20xx, we will carry out institutionalized management.

According to the department management system, we will formulate detailed management rules for the Department of Medicine and Devices to make the system detailed, organized and shift-based.

IV. Pay attention to talent cultivation and improve the quality of personnel in the pharmaceutical and medical department.

With the development of modern medicine, the work of the Department of Pharmacy and Devices has evolved from simple to complex, and the disciplines we face are constantly expanding. This requires our staff in the Department of Pharmacy and Devices to continue to learn and update their knowledge. The current staff of our department is uneven, and staff training is an important task. According to the job responsibilities of personnel at all levels in the Pharmaceutical and Devices Department, we must carefully organize and implement it, and conduct strict assessments. Only by doing a good job in personnel training and improving the professional quality and technical level of all staff can we better complete various practical tasks and ensure the implementation of various systems in the Pharmaceutical and Devices Department.

Comrades, looking back and summarizing the past year, we plan to look forward to the coming year. We are full of confidence. We must face the challenges and opportunities of medical reform and provide suggestions for the development of the department. We must actively innovate. Work ideas, work together, and work together to make new and greater contributions to the development of the pharmaceutical industry in our hospital. 2020 Pharmaceutical and Equipment Work Summary 4

Time has passed, and it has arrived at the end of 20xx in the blink of an eye. . Looking back on this year's work, I can simply summarize it as "no major mistakes and no innovations". Below I will give some detailed examples and plan for the next year's work.

1. Summary of this year’s work:

1. Inspection by the superior authority: With the care and support of the hospital leaders and brother departments, and the concerted efforts of the department members, Next, the 20xx annual pharmaceutical quality control inspection was successfully passed. Problems discovered during the inspection, such as "the prescription of semen and anesthetic drugs were not serialized, the labeling of high-risk drugs was not standardized enough, and the abuse of antibacterial drugs. Problems that could be solved by themselves have been rectified, and problems that could not be solved by themselves were also reported in writing."

2. Work system implementation: The implementation of systems related to pharmaceuticals and devices, such as "Pharmaceutical Administration Committee Responsibilities, Prescription Review Management, Medical Special Drug Management System", etc., are relatively superficial. In order to adapt to the new form All should be improved.

3. Work errors: errors include "planning errors, medication delivery errors, recording errors", etc. Although the error log does not record any errors, I believe it is not true that there are no errors. () Slow-selling drugs were not discovered and disposed of in time, unsalable drugs were not reported in time, prescription drug A was mistakenly issued as drug B, prescriptions were unreasonable and no timely intervention was made, prescriptions were not classified and bound as required, Chinese medicine pieces were not maintained according to standards, etc.

4. Supply of medicines and equipment: As a secondary department, the Pharmacy Department also serves the clinical departments with patients as the center, basically ensuring the needs of the department; however, due to various factors, it does not actively recommend new varieties to the clinic (patients Except for temporary purchases). In general, our department has not performed its duties and obligations well

5. Supplier management: Supplier drugs in 20xx: Zhejiang Yingte Pharmaceutical, Huadong Medicine. New Special Drugs, Zhejiang Shangyu Xinxin Pharmaceutical, Zhejiang Huatong Pharmaceutical, Jiuzhoutong Hangzhou Pharmaceutical Company, Zhejiang Fulinmen Pharmaceutical, and Zhejiang Haodelei Pharmaceutical are the main ones; traditional Chinese medicine preparations include Xiaoshan Pharmaceutical Traditional Chinese Medicine Branch, Hangzhou Materia Medica (newly added) Unit); equipment and consumables categories include Shanghai Hongchang Biotechnology, Jiangxi Magotan Industrial (the name of the unit has been changed, the operator remains the same), Henan Yadu, Henan Renli (the operator is Dunjuntang, the original Henan Yadu has stopped supplying), Hangzhou Letong and Yichun Dade Trading (newly added, no qualification certificate has been provided for operating Class III high-risk devices). Among the above suppliers, Shanghai Hongchang Biotech operates beyond the scope (unqualified to operate pharmaceutical reagents); Jiangxi Magotan and Henan Provincial Renli are both. Part-time operation; Hangzhou Letong and Yichun Dade trading parties' procedures should be timely and standardized (key supervision objects)

6. Voice from outside the department: The main feedback problem is "out of stock again!" ","The manufacturer or specifications have changed again! ", "How much more expensive is the price (selling price) of a certain drug than elsewhere?"

2. Major newly implemented regulations on drugs and devices:

Regulations on the Supervision and Administration of Medical Devices (State Council Order No. 650 No.): It was revised and adopted at the 39th executive meeting of the State Council on February 12, 20xx. The revised "Regulations on the Supervision and Administration of Medical Devices" are now announced and will come into effect on June 1, 20xx.

3. Work plans and goals for the coming year

In the second half of this year, I participated in several trainings organized by the Food and Drug Administration. To sum up, the main contents are "review of supplier qualifications, drug and device "Precautions for acceptance, monitoring and reporting of adverse drug and device reactions or events, and antimicrobial drug management". It can be seen that the management focus of the competent authorities in 20xx, therefore, we must also include these in the planned key management. The details are as follows:

1. Re-examine the qualifications of each supplier, focusing on suppliers operating pharmaceuticals and third-class medical devices; report risk suppliers to the supervisor in a timely manner and give evaluations and processing opinions.

2. Strengthen the management of medical-specific drugs: regularly organize relevant management personnel to supervise and inspect the purchase, storage, and use of sesame drugs throughout the hospital; regularly conduct inspections of relevant personnel on relevant laws, regulations, ethics, Professional skills training.

3. Strengthen the management of antimicrobial drug use: timely adjust the antimicrobial drug catalog of our hospital based on the drug monitoring results of Zhejiang Province, the antimicrobial drug catalog, and the antimicrobial drug management system of our hospital; promptly report the use of antimicrobial drugs;

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4. Strengthen prescription evaluation: According to the hospital prescription evaluation specifications, 100 outpatient Western medicine and Chinese medicine prescriptions will be selected for evaluation each month, and the evaluation results will be reported.

5. Strengthen communication among department members and between departments to avoid work differences affecting the entire group and affecting work.

The plan is only part of the plan and cannot arrange all activities. I hope that at this new starting point in 20xx, we can do better and the hospital will be bigger. 2020 Pharmaceutical and Device Work Summary 5

Under the correct leadership of the hospital leaders, all employees of the Pharmaceutical and Device Department have established the guiding ideology of “patient-centered and serving the people wholeheartedly”, corrected their service attitude, and transformed the Pharmaceutical and Device Department’s Each work is carried out in an orderly manner, and the work at this stage is summarized as follows:

1. Taking the establishment of a second-level hospital as an opportunity, use hospital accreditation standards to drive the work of the department and further standardize various types of work in the department personnel responsibilities, and gradually establish and improve the structure of the pharmacy department of secondary hospitals.

2. Strengthen the management of the department, organize regular training and learning for department personnel, and improve window service skills and attitudes.

3. Strengthen the hospital’s pharmaceutical management, organize and convene meetings of the Pharmacy Management and Drug Therapeutics Committee on a regular basis, report the medication status of each department in the hospital, and guide each department in the hospital to use medication rationally. This will prevent the occurrence of any drug-induced accidents and ensure the rationality and safety of clinical medication in hospitals.

4. Actively implement the "Regulations on Prescription Management", further improve the evaluation of outpatient prescriptions, and promptly discover and correct the irrational use of drugs by doctors.

Actively participate in prescription reviews organized by the Bureau of Health and Family Planning, and promptly correct problems existing in the reviews. Review hospital prescriptions every month, point out unreasonable prescriptions in a timely manner, and communicate with relevant doctors to improve the quality of hospital prescriptions.

5. Implement the reporting, monitoring and management of adverse drug reaction information in our hospital by formulating quantitative indicators for the collection of adverse drug reaction information in each department.

This quarter, 2 cases of adverse drug reaction reports have been completed.

6. Continue to implement the national essential medicine system in our hospital, organize and implement online procurement of essential medicines and sunshine points application, and strictly implement zero-margin sales of medicines. This quarter, online purchasing of essential medicines and sunshine points have met relevant requirements.

7. In accordance with the requirements of the "Measures for the Management of Clinical Application of Antimicrobial Drugs", continue to organize and carry out management work related to the use of antimicrobial drugs in hospitals, carry out evaluation of medical orders for antimicrobial drugs in hospitals, and gradually improve the level of rational use of antimicrobial drugs by doctors in our hospital. Reduce the percentage of antimicrobial drug use among hospital outpatients and inpatients. Control the use of antibacterial drugs within prescribed limits.

8. Keep abreast of the demand for drugs and equipment in various departments, understand the feedback information after the use of drugs and equipment, purchase and reserve relevant drugs and equipment in a timely manner, and ensure the timely supply of drugs and equipment in clinical departments. Summary of Pharmaceutical and Device Work in 2020 6

In 20xx, our hospital implemented the basic drug system, conscientiously implemented the "Drug Administration Law", "Pharmaceutical Management Regulations for Medical Institutions" and other relevant laws and regulations. The care of the leaders in the hospital Under the direct leadership of the hospital and the dean in charge, with the strong support of relevant functional departments and departments, and closely focusing on the work priorities and requirements of the hospital, all employees have pioneered and innovated and worked hard with a spirit of unity, collaboration, truth-seeking and pragmatism. , the hospital’s pharmaceutical and equipment work has made significant improvements. The work of pharmaceuticals and equipment in the past six months is summarized as follows:

1. According to the "National Essential Drugs List" and "Quality Management Practices for Drug Procurement and Supply", combined with our hospital's medication habits and actual clinical needs, at the same time, in During the supply of drugs, we pay attention to information, regularly analyze and compile statistics on the drug use of each department and provide rapid feedback, prepare a reasonable procurement plan, and submit it to the dean in charge for approval before centralized procurement to ensure timely and effective clinical drug use.

2. Pay close attention to the quality of drugs, adhere to the system of drug procurement, acceptance, storage, and maintenance, and insist on conducting spot checks on the quality of drugs and consumables in pharmacies and drug stores once a month to ensure the quality of drugs. . And adhere to the basic principle of first-in-first-out for warehouses and pharmacies.

3. Do a good job in statistics and summary of relevant data, and complete monthly reports in a timely manner (inventory of warehouses, pharmacy drugs, and consumables every month). Cooperate with the Finance Department to improve the drug proportion control plan.

There is currently a problem: Laparoscopic instruments such as grasping forceps, biopsy forceps, etc. in the operating room on the sixth floor were not cleaned properly, resulting in clogging of the instruments. They have been sent to the manufacturer for cleaning (the manufacturer requires cleaning fees). Because the operating room The equipment is relatively delicate, and some of the equipment is imported. In order not to affect the service life of the equipment, I personally recommend that you purchase an ultrasonic cleaning machine immediately.

Work plan for 20xx:

1. Implementation Drug catalog, rationally formulate drug procurement plans, organize and implement them after approval by the dean, ensure timely clinical use of drugs, and strengthen and improve the file update and evidence validity management of drugs, consumables, reagents, and equipment.

2. According to clinical needs, purchase some large-scale medical equipment, such as defibrillators in the rescue room, hysteroscopy system equipment in the operating room, and ultrasonic cleaning machines in the operating room on the sixth floor. Improve the file management of newly purchased equipment, do a good job in equipment maintenance, regularly check and inventory equipment, and ensure that the accounts are consistent. Summary of Pharmaceutical and Device Work in 2020 7

In 20xx, under the leadership of the Bureau’s party group, the Bureau’s inspection team, in accordance with the work policy of “taking supervision as the center and combining supervision, assistance and promotion”, did a lot of work in the supervision of pharmaceutical and device A lot of fruitful work has been done to ensure the safety and effectiveness of medication for the broad masses of people in our county.

At present, there are 10 drug business units and drug user units within the jurisdiction of our county. Among them, drug wholesale units, drug retail stores, township health centers, county hospitals, individual clinics, village clinics, and other medical institutions.

In 20xx, the drug and device supervision work of the bureau’s inspection team can be summed up in one sentence, that is: adhere to one center and achieve two clarifications.

In 20xx, the bureau’s inspection team worked in the bureau Under the leadership of the party group, in accordance with the work policy of "centering on supervision and combining supervision, assistance and promotion", a lot of effective work has been done in the supervision of pharmaceuticals and devices, ensuring the safety and effectiveness of medication for the broad masses of the people in our county.

At present, there are ** drug business units and drug user units within the jurisdiction of our county. Among them, drug wholesale units, drug retail stores, township health centers, county hospitals, individual clinics, village clinics, and other medical institutions.

In 20xx, the drug and device supervision work of the Bureau’s inspection team can be summed up in one sentence, that is: adhere to one center, achieve two clarifications, three combinations, grasp the four focus points, and adhere to the "five no's" Let it go”. Specifically speaking, adhering to a center means adhering to supervision as the center.

The second clarification is to clarify the work goals and clarify the work priorities. At the beginning of this year, based on the actual situation of our county, the bureau leaders determined this year's work goals: first, the order of drug circulation has improved significantly; second, the production and sale of counterfeit and inferior drugs has been effectively curbed; third, the classified management of drugs in the circulation field has been fully implemented; fourth, First, drug advertising is standardized and orderly; fifth, drug use at the grassroots level in rural areas has been significantly improved. While formulating work goals, the work focus was further clarified, that is, focusing on rectifying the rural drug market to ensure safe and effective drug use by rural people. The three combinations are the combination of special rectification and daily supervision, the combination of treating symptoms and root causes, and the combination of strict law enforcement and scientific management. We must grasp four focus points, that is, in the work of rectifying and standardizing market order, we must firmly focus on banning illegal markets, investigating and punishing illegal operations, cracking down on illegal and criminal activities that produce and sell fake and inferior drugs, and standardizing the business behavior of enterprises. . Five, don’t let go: don’t let go until the case is clarified; don’t let go if the source and flow are not identified; don’t let go if those who produce and sell counterfeit goods are not dealt with according to law; don’t let go if those who should be transferred to judicial organs are not transferred; don’t let go if they are shielding and condoning Officials involved in the production and sale of counterfeit and substandard drugs will not be let go without being held accountable.

Since the beginning of this year, we have inspected more than one drug-related unit, opened a case, and closed the case. We have rectified the remaining units within a time limit, dispatched inspections per person, and confiscated all specifications and varieties of pharmaceutical equipment, and the value of the goods. Ten thousand yuan, fine. Ten thousand yuan. At present, the drug supervision work in our county is being further in-depth, and supervision is continuously increasing to ensure the quality of medicines and equipment, ensure the safety and effectiveness of medicines for the people of the county, and safeguard the healthy development of a well-off society in the county.

Combining the three, grasping the four focus points, and adhering to the "five don't let go". Specifically speaking, adhering to a center means adhering to supervision as the center. The second clarification is to clarify the work goals and clarify the work priorities. At the beginning of this year, based on the actual situation of our county, the bureau leaders determined this year's work goals: first, the order of drug circulation has improved significantly; second, the production and sale of counterfeit and inferior drugs has been effectively curbed; third, the classified management of drugs in the circulation field has been fully implemented; fourth, First, drug advertising is standardized and orderly; fifth, drug use at the grassroots level in rural areas has been significantly improved. While formulating work goals, the work focus was further clarified, that is, focusing on rectifying the rural drug market to ensure safe and effective drug use by rural people. The three combinations are the combination of special rectification and daily supervision, the combination of treating symptoms and root causes, and the combination of strict law enforcement and scientific management. We must grasp four focus points, that is, in the work of rectifying and standardizing market order, we must firmly focus on banning illegal markets, investigating and punishing illegal operations, cracking down on illegal and criminal activities that produce and sell fake and inferior drugs, and standardizing the business behavior of enterprises. . Five, don’t let go: don’t let go until the case is clarified; don’t let go if the source and flow are not identified; don’t let go if those who produce and sell counterfeit goods are not dealt with according to law; don’t let go if those who should be transferred to judicial organs are not transferred; don’t let go if they are shielding and condoning Officials involved in the production and sale of counterfeit and substandard drugs will not be let go without being held accountable.

Since the beginning of this year, we have inspected more than one drug-related unit, opened x cases, and closed x cases. We have rectified more than one company within a time limit, dispatched inspections per person, and confiscated all specifications, varieties, and values ??of pharmaceutical equipment. Ten thousand yuan, fine. Ten thousand yuan. At present, the drug supervision work in our county is being further in-depth, and supervision is continuously increasing to ensure the quality of medicines and equipment, ensure the safety and effectiveness of medicines for the people of the county, and safeguard the healthy development of a well-off society in the county.