Summary is a kind of written material to review and analyze the study, work or completion of a certain stage afterwards, which can effectively exercise our language organization ability. Write a summary. So what is the format of the summary? The following is a summary of the work of drug reviewers carefully compiled by me, hoping to help everyone.

Work summary of drug assessor 1 1, adhere to the principle of quality first, check the quality of drug distribution, and take the main responsibility for the quality of drug distribution.

3, according to the invoice batch audit outbound drugs, to achieve accurate quantity, good quality, strong packaging, clear signs;

4, the special management of drug distribution should be carefully checked;

5. For drugs with qualified quality, affix the special stamp for outbound inspection and sign it; Drugs subject to electronic supervision should be scanned and uploaded.

6, for unqualified drugs, should suspend delivery, take effective control measures, reported to the quality management agencies for quality review;

7, in the computer management system for outbound check operation.

8. The outbound review record includes the common name, dosage form, specification, quantity, batch number, expiration date, manufacturer, outbound date, quality status and reviewer of the purchasing unit and drug, which is convenient for quality tracking and record keeping for more than five years.

Work Summary of Drug Reviewer 2 I officially joined the company's acceptance team in March of 20xx and participated in the company's drug warehousing acceptance. In the meantime, we have constantly strengthened our understanding of drugs. Under the enthusiastic guidance of colleagues and leaders in the company, I learned about the overall situation of the company, the workflow of the department and the positions to be engaged in one by one, and actively participated in related work. According to the actual work, I have completed the knowledge of drug warehousing, drug acceptance, drug transportation and drug audit with theoretical knowledge. At the same time, I also participated in the staff training of the quality control department, which made up for some lack of knowledge. Now I will sum up some problems encountered in my work.

First, the better aspects to be completed this year are:

1, actively participate in the training of departments, make up for some lack of knowledge, and have a better understanding of drugs;

2. Master the main responsibilities of the acceptance post and the specific operation of daily work, and have a deeper understanding of the drug acceptance work;

3, can independently solve some problems and difficulties encountered in the work. For example, the correction of mistakes in operation, some consultations from customers and other daily problems;

Second, some places need to be corrected:

1, the mastery and use of daily computer systems need to be strengthened.

2. The knowledge of drugs needs to be strengthened; In particular, the acceptance and treatment of special drugs need further study by the leaders of quality control department.

3. In the process of drug acceptance, errors still exist, and daily operation errors cannot be effectively avoided; Mainly reflected in these aspects: drug warehousing acceptance is a very important link. After the drugs arrive, the consignee should adhere to the principle of "quality first" and strictly control the quality of drugs to prevent counterfeit and inferior drugs from flowing into the enterprise. Drug quality acceptance should be carried out in accordance with the acceptance procedures and quality acceptance rules. Drugs returned after purchase and sale shall be inspected according to varieties, specifications and batches, and inspection shall not be missed. Inspectors must carefully record the drug warehousing acceptance, and record it item by item according to the supplier, quantity, arrival date, product name, dosage form, specification, approval number, batch number, manufacturer, expiration date, quality status, acceptance conclusion, qualified quantity, acceptance date, inspector and other contents, and record the electronic documents, which should be true, complete and traceable and kept for at least five years. The inspector accepts the drugs with the certificate issued by the supplier's peers with the goods. The certificate is not handwritten, but an original computer bill stamped with the supplier's special seal for drug distribution. The acceptance of special drugs does not meet the relevant regulations of special drugs, and there is no specific acceptance procedure for special drugs on the computer. The understanding and mastery of special drugs need to be further strengthened. There is no complete acceptance record for the drugs that need to be refrigerated, and the temperature and humidity data are not monitored and recorded in time when the refrigerated drugs arrive. The acceptance of unqualified drugs did not specify the treatment measures in detail.

Stone. The acceptance of imported drugs shall be accompanied by the registration certificate of imported drugs, the inspection report of imported drugs and the customs clearance form of imported drugs, and stamped with the fresh seal of the quality control institution of the transferring unit. Imported preventive biological drugs and blood products should be "healthy"

Product import approval document, and stamped with the red seal of the quality control institution of the transfer unit. Disposal of returned drugs; After receiving the Notice of Returning Drugs, the inspector must re-examine the returned drugs, and only after passing the inspection can he enter the qualified product area for acceptance and warehousing management of compound preparations containing ephedrine. The inspection team of the Quality Management Department is responsible for acceptance of compound preparations containing ephedrine to ensure that the tickets, accounts and goods are consistent. After the arrival of such drugs, inspectors should distinguish such drugs in time according to the ingredients marked in the drug instructions, and put them into the waiting area of the corresponding warehouse according to their storage conditions. After such drugs are physically accepted according to the acceptance procedures, they shall be promptly notified to the Logistics Department for warehousing. And set up a special area containing ephedrine compound preparations in the warehouse to store such drugs centrally, and set up obvious signs. Clarify the responsibilities of examiners: consciously learn the knowledge of pharmaceutical business and drug supervision and management regulations, and strive to improve the acceptance skills. In this respect, we need to strengthen our study and make up for the shortcomings in our work. There are still many areas to be improved in the electronic supervision of drugs, which are mainly reflected in the following aspects: (1) there are some differences between the drugs stored in the supervision network and the actual inventory; Due to the imperfect addition of inter-bank units, data cannot be uploaded to the supervision network center in time due to network relations. I don't have a deep understanding of the arrangement of documents and its importance, and there are still many remnants of the classification of various drugs and the custody of drug testing.

Three. I have accumulated experience and lessons in more than half a year's work in 20xx, hoping to improve myself in my future work. This plan is specially formulated:

After work, take some time to strengthen the study of pharmaceutical knowledge to make up for my own shortcomings in pharmacy;

In the process of work, constantly improve their work skills and strive to do well.

Medical services to better complete daily work;

Try to understand the arrangement and importance of documents, the classification of various drugs, the custody of drug trials, etc.

Draw lessons from the past, carefully check drug information, reduce drug acceptance errors, make statistics and classification of existing errors, and strive to achieve the requirement of zero errors.

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