Year-end summary of drug quality administrator
With the care and support of hospital leaders, in the past year, I have worked hard, been modest and prudent, constantly improved myself, and strived to improve my professional ability and service consciousness, and achieved the following results.
First, actively participate in the business study and professional examination organized by the hospital to improve the business level.
Two, timely grasp the development of new drugs, often introduce new drugs to clinicians, and gradually update the varieties and dosage forms of drugs according to clinical needs.
Third, there is a sense of responsibility in work, drugs are stored neatly and placed in categories; Drug distribution should be strict and serious, and medical insurance policies should be strictly controlled. When problems are found, doctors should be contacted in time to prevent mistakes and accidents.
Fourth, actively participate in different learning activities organized by the center, and maintain a high degree of consistency with the main ideas of superiors.
Five, to ensure the efficacy and quality of drugs, to ensure the safety of clinical medication; Timely report expired and deteriorated drugs and deal with them according to regulations.
Six, strengthen service awareness, improve service quality, and achieve patient satisfaction, leadership satisfaction and self-satisfaction.
Achievements belong to the past, and I will make persistent efforts, work hard and strive for greater achievements in the new year.
Year-end summary of drug quality administrator II
In XX years, our station still carried out quality management around the requirements of national monitoring technical specifications and the requirements of sampling, analysis and control of daily environmental quality control in Jiangsu Province, aiming at enhancing the quality awareness of employees and improving the quality of monitoring work. According to the relevant technical regulations and requirements of national and provincial environmental monitoring quality assurance, total quality management was implemented in the whole process of monitoring work, which played a certain role in ensuring the accuracy and effectiveness of monitoring data.
This year's quality management is summarized as follows:
First, consolidate the achievements of laboratory accreditation and qualification recognition.
At the beginning of XX, our station successfully passed the national laboratory accreditation and laboratory qualification accreditation re-evaluation. This year, with the aim of consolidating the achievements of laboratory accreditation and qualification, and based on the quality system documents, our station comprehensively studied and implemented the new ISO/IEC 17025 laboratory competence accreditation criteria, and comprehensively and seriously rectified the nonconformities in this year's supervision and evaluation work. It ensures the applicability and effectiveness of the quality system documents of our station. For the newly purchased instruments and equipment, relevant operating procedures are also written in time to ensure that the monitoring work of our station can run continuously and effectively in accordance with the ISO/IEC 17025 accreditation criteria.
Two, organize business learning job training, improve the professional quality of all staff.
According to the business study plan made this year, the key points of Taizhou quality control work in 2008 and the quality management work plan of this station, we have carried out the study on the basic knowledge of environmental monitoring, the application of quality assurance and quality control technology, and the laws and regulations related to water pollution prevention and control law, and organized the staff of the whole station to continue to study the ISO/IEC 17025 laboratory competence accreditation criteria. By strengthening the professional learning of monitoring personnel, the professional quality of monitoring personnel has been significantly improved.
While doing a good job in self-study, actively participate in various classes and training courses organized by higher authorities. In the whole year, 14 people participated in the training of laboratory qualification internal auditor, laboratory qualification evaluation, news article writing training, motor vehicle exhaust detection training, nuclear and radiation monitoring training, practical application of automatic monitoring system for pollution sources, and analysis of volatile organic compounds in water, soil and air. It laid a foundation for improving the monitoring ability of our station and broadening the monitoring field.
Third, actively participate in activities such as ability verification, appraisal and skill competition organized by higher organizations.
This year, our station actively organized relevant personnel to participate in the laboratory comparison of volatile phenol and total nitrogen in water quality organized by Jiangsu Environmental Monitoring Center in 2008, the ability verification of five inorganic salts in water organized by China National Accreditation Committee for Conformity Assessment, and the monitoring skill competition of Taizhou Environmental Monitoring System. The comparison results were all qualified at one time, and the ability verification results were not notified. In the monitoring skill competition, Xu won the first place in the group and the third place in the theoretical competition, and was an excellent player in the monitoring skill competition.
Four, strict quality control, improve the quality of monitoring work.
In order to continue to strengthen the standardized construction of on-site monitoring and pollution source monitoring and effectively control the quality of on-site sampling, this year, based on last year's quality control, combined with the specific requirements of environmental monitoring quality control samples implemented in our province, we continued to implement corresponding on-site sampling and pollution source monitoring quality control measures, and effectively controlled the monitoring quality of our station through the application of quality control measures such as blank on-site whole process, on-site parallel samples, indoor parallel samples, standard recovery, quality control chart and standard sample comparison.
In the whole year, 7582 quality control materials were completed, with an inspection rate of over 20% and a qualified rate of over 97%. Among them, there are 2 1 16 parallel samples; 2327 indoor parallel samples; 19 1 1 recycling samples; 9 standard samples; The whole program has 12 19 spaces. The quality control sample inspection rate and quality control data qualified rate all meet the relevant quality control requirements of the province.
Year-end summary of drug quality administrator III
1. Abide by post responsibilities, take the initiative to learn, master work skills, and be more competent for quality control;
(1) Be responsible for drug quality management under the leadership of the manager of quality management department.
(2) Supervise and guide the company's drug procurement, acceptance, storage, maintenance, sales and transportation process, and promote the standardized operation of the company's quality management.
(3) Be responsible for the preliminary examination and filing of the first camp varieties and enterprise data.
(4) Effectively manage documented suppliers, including their quality reputation and licensing qualifications. Report the existing problems to the manager of the quality control department in time, and inform the purchasing department in time to ask for expired or missing qualifications.
(5) Seriously implement daily work according to GSP.
(6) Collect the latest drug information and report it to the manager of quality control department.
(7) Do a good job in collecting and reporting adverse drug reactions.
(8) Other tasks assigned by the manager of quality management department and superior leaders.
Second, strive to improve work efficiency and complete the work with good quality and quantity.
First of all, make a good daily work plan and coordinate the daily work according to the priorities.
Row, and strive to achieve the best results.
Secondly, enhance their ability to deal with and solve emergencies.
Finally, pay attention to the coordination and communication between colleagues, dredge the workflow, and avoid the impact or even loss of business work caused by poor coordination.
Third, the existing shortcomings and the direction of future efforts.
While seeing the progress, I am also clearly aware of my own shortcomings. In the future, we should communicate more with the competent leaders, face up to our own shortcomings, challenge ourselves, and strive for a breakthrough in our work in 20XX.
Fourth, the work plan for next year
On the basis of work summary in 20XX, I will strengthen in the following aspects in 20XX:
1, strengthen the quality management standard of pharmaceutical business;
2. Collect drug quality information and take every feedback seriously;
3. Do a good job in company quality training;
4. Establish scientific and strict file management.
Suggestions of verb (abbreviation of verb) on company development and quality management.
In daily work, we should also pay attention to performance management in all aspects of drug quality assurance. There must be relevant implementation regulations and operational specifications from the aspects of procurement, delivery (delivery), acceptance (rejection), storage (loss reporting), maintenance, delivery, outbound audit, outbound transportation, sales return and purchase return, and then there must be corresponding performance appraisal. Through effective supervision measures, the dynamic management of everyone's work performance is implemented. Pay full attention to the control of each working link and working procedure by strengthening the consciousness of norms; Pay full attention to the importance of business standardization and drug quality by strengthening quality awareness; By strengthening the awareness of efficiency, we can pay full attention to the optimization of various work contents and working methods. I think that through the implementation of effective performance management, we can greatly mobilize everyone's work enthusiasm and promote the improvement of everyone's overall work quality, thus promoting the promotion of the company's core competitiveness.
Year-end summary of drug quality administrator IV
Time flies, time urges us to bid farewell to 20XX, and hopes to inspire us to achieve new heights in 20XX. Looking back on the coming year, opportunities and challenges coexist, and the certification of the new GSP will undoubtedly bring great changes to pharmaceutical companies. 20XX has been preparing for the new GSP certification for half a year. In the process of reporting GSP application materials in the early stage, the nonconformities proposed by the leaders of the provincial bureau were seriously rectified and reported to the provincial bureau as soon as possible after rectification. This process was repeated, but no effort was made, and the GSP certification data was declared successfully. On July 20XX 1 -2, the company welcomed the new version of GSP certification. Certification staff, the provincial bureau, made a careful inspection of our company and gave us the most specific and impressive lesson on drug quality. The certification process is tense and happy, and it is worthwhile to see the approval of the leaders of the provincial bureau for our work in the past year. In short, through the efforts, cooperation and continuous progress of various departments, the company has completed the certification of the new GSP and basically completed the normal work tasks of the company this year.
In order to better complete the work, sum up experience, foster strengths and avoid weaknesses, the work of the past year is summarized as follows:
1, conscientiously implement the spirit of the documents and work arrangements of the State and Provincial Food and Drug Administration, actively cooperate with the relevant inspections of the Municipal Bureau in addition to doing a good job in drug quality audit and supervision, and urge the effective implementation of rectification. Under the leadership of the company and the supervision and management of the US Food and Drug Administration, we have done a good job in the quality management of drugs handled by the company, and achieved legal operation and standardized operation.
2. In order to ensure the quality of the drugs handled by our company, according to the requirements of GSP, the first-time enterprises and the first-time varieties were strictly audited. Establish the audit and file of the first battalion enterprise and the first battalion variety. 9 first-time enterprises were audited, and the first-time varieties were 1 1. In addition, in the computer management system, the qualification of suppliers is effectively managed, and the missing information is reported to the purchasing department in time to ensure the legal operation of drugs.
3. Fully grasp the dynamics of drug quality in the whole company, establish an electronic file catalogue by classification, and provide customers with various quality information quickly, such as variety qualification, company qualification and drug price.
4. Collect and transmit the quality information documents of the Food and Drug Administration accurately and timely, analyze and summarize them, transmit them in time, and feed them back to all departments in the form of quality information transmission sheets and copies to ensure the timely and smooth transmission of quality information and the accurate and effective utilization.
5. Under the leadership of the quality control minister, participate in the review, confirmation and loss reporting of unqualified drugs, control unqualified drugs and reduce the generation of unqualified drugs. The summary and analysis of unqualified drugs were completed.
6, guide and supervise the quality work in the process of drug storage, acceptance, maintenance and storage, and make a complete record, regularly evaluate the implementation of the quality system every month.
7. Under the leadership of the quality control minister, participate in and complete the verification of the company's cold storage.
8. Supervise and manage the delivery and storage of the electronic codes of drugs operated by our company. The state stipulates that drugs without electronic codes may not be purchased, and assists the storage and transportation departments in dealing with problems encountered in electronic supervision.
9. Successfully completed the filing of company salesmen, the issuance of company licenses and the issuance of legal person power of attorney.
10. under the guidance of the minister, I am familiar with the quality inquiry and registration report, and now I can complete it independently.
1 1, to assist the quality evaluation of purchased drugs.
12. Computer permission check has been completed.
20XX is a whole year, and it is also an extraordinary year for me, and it is also a year of harvest. Watching the baby grow up little by little this year, it is not easy to understand the company leaders here. The growth of the company is inseparable from their good intentions. I want to thank them for providing all of us with this platform for rapid growth. Thank you!
Looking back on the past and looking forward to the future, in 20XX, facing the new challenges, the reform of the pharmaceutical industry and the changes in the company's internal policies, quality management has a glorious mission and great responsibility. With the correct leadership of the company and the joint efforts of colleagues, we will further invigorate our spirits, unite as one, ensure the quality and safety of drugs with a better mental state, a more solid and meticulous work style and faster work efficiency, and make new contributions to the company faster and better.
Problems existing in the work:
1, to strengthen their own learning, for some unknown quality problems, ask Minister Xue and the company's superior leaders for advice, and solve all kinds of problems in time and accurately.
2, should arrange their own work plan, conscientiously do a good job summary. We should carefully analyze the mistakes in our work to avoid making mistakes again.
3. Work efficiency should be improved, and the work cannot be delayed, and the work of the day should be completed on the same day.
4, the work can not be done, it is over, you should do it seriously.
5. Be more careful about the qualification examination of units, varieties and customers. After the license is changed, it should be obtained from the purchasing and selling unit in time, and the qualification should be obtained in advance when it expires to prevent the qualification from being illegal and non-compliant.
6, maintenance acceptance records to see more, found that the error, remind acceptance maintenance personnel timely acceptance maintenance.
7, electronic supervision code should be carefully checked, billing must be checked.
8. Look for mistakes in the monthly self-examination. The more, the better. You cannot be too careful.
9, quality management system documents found errors should promptly notify the relevant personnel to make changes.
10, the application materials should be carefully checked, and the warehouse area should refer to the last application materials and personnel.
1 1. After personnel changes are made, employment permits are obtained or online filing is made in Shandong Province, relevant departments and personnel (such as those in the Medicine God) shall be notified in time.
12, the specifications, approval number and other information in the drug commodity file should correspond to the drug standard and be carefully checked.
Year-end summary of drug quality administrator V
Time flies, another year has passed in a blink of an eye, and it has been more than a year since I came to Xingbei Pharmaceutical Chain. With the enthusiastic help of leaders and colleagues, I am now familiar with the work of the quality control department. Here, I would like to express my heartfelt thanks to the leaders and colleagues of the company! Thank you for your support and cooperation in my work, so that I can successfully complete all the work. In the past year's work, I have done all the work conscientiously and responsibly in strict accordance with the company's management system and GSP requirements. Now I will summarize the work in 20xx as follows.
1. Under the leadership of General Manager Liu, first of all, we know who I work for and how to do my work well, which gives me a new understanding of my work. Working is not for others, but for myself, which strengthens my sense of responsibility and improves my comprehensive quality. Secondly, I studied the _ _ Anniversary of the Founding of the Party, Corporate Culture and Song of Revitalizing the North, which strengthened the construction of revitalizing the northern corporate culture and made it more colorful, reflecting President Liu's far-sighted and enterprising spirit and his humanistic care for the employees of the company.
2. Seriously implement the document spirit and work arrangement of the national and provincial US Food and Drug Administration, and do a good job in the drug management of our company under the supervision of the municipal US Food and Drug Administration, so as to operate according to law and standardize operations.
3. In order to ensure the product quality of our company, according to the requirements of GSP and its normative documents, the first-time enterprises and first-time varieties are strictly audited, and the files of first-time enterprises and first-time varieties are established, and 36 files of first-time enterprises are established in 20xx.
4. Supervise the standardized management of suppliers' outbound orders, urge the purchasing department to classify relevant bills in chronological order and suppliers, and supervise the purchasing department and suppliers to improve the correction procedures of varieties with inconsistent batch numbers to ensure the quality of products purchased by the company and prevent errors in drug circulation.
5. According to the requirements of GSP, all aspects of procurement, sales and storage are strictly implemented in accordance with GSP, and the quality of drugs runs through the whole process of procurement, sales and storage, actively cooperating with stores to issue the sales outbound list to stores in time. In all aspects of procurement, sales and storage, we always adhere to the principle of "quality first", ensure that our own drugs are qualified, ensure the safety of public medication, ensure the company's good quality reputation, and buy conscience drugs with gratitude.
The work plan of 20xx is to try to correct the shortcomings in the work and make GSP run well and continuously. All records of GSP shall be recorded in strict accordance with GSP requirements, properly kept and checked.
20xx review for half a year, the task is very heavy. I hope that all departments will actively support and cooperate, give full play to team spirit and make full preparations for review.
In order to ensure the smooth progress of the work in 20xx, I will take enterprise development as my own responsibility, work hand in hand with my colleagues, strengthen communication with all departments, make overall arrangements, and strive to achieve the successful completion of the work in 20xx.
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