本偏差是由于标准品管理员一时疏忽，拿错标准品；而检验员王昊未核对标签信

This deviation is due to the carelessness of the standard product administrator, and the wrong standard product was taken; but the inspector Wang Hao did not check the label information, which led to the use of the standard product and caused the abnormal peak time. <br><br>1. This deviation is caused by human error. The peak time of the standard is abnormal due to the wrong use of the standard. The deviation pattern is consistent with the impurity peak of the retesting result of the original solution, but the experimental result cannot be calculated. A test report is issued based on the retest results of the sample stock solution. This deviation has no effect on product quality evaluation. <br>2. Investigate the experimenter's experiment in the past year, and no similar errors have occurred. It is also the first time that the laboratory has used a standard error in the past two years. If the standard product is used incorrectly, it will be found in time and the risk is controllable; therefore, the product batch quality risk detected by the experimenter in the early stage is controllable. <br>3. Checking the standard product manager Cheng Wenxian is also the first time such a deviation has occurred and the risk is controllable. <br><br>1. The test results of the three batches of HS-25-I samples shall be void and retained, and a test report shall be issued based on the results of the retest of the original liquid. <br>2. Train relevant personnel on the H0-SOP-72013 standard management program version 01, emphasizing: before using the standard, the analyst needs to check whether the standard packaging is intact and check whether the information on the label is correct.

This deviation is due to the standard product administrator for a moment's negligence, take the wrong standard product, and the inspector Wang Wei did not check the label information, resulting in the use of standard products error, resulting in peak time anomalies, is a human error. <br><br>1. This deviation is caused by human error, due to the use of standard products lead to the standard peak time anomaly, deviation map and the original liquid retest results of impurity peak consistent, but the experimental results can not be calculated, this experimental map waste reservation for reference only, to sample the original liquid retest results issued a test report, this deviation has no effect on product quality evaluation.<br>2. The experimenter's experiment in the last year did not make a similar error, and it was the first time in the last two years that the laboratory had the wrong deviation in the use of standard products. If the standard product slots incorrectly, it will be found in time, the risk can be controlled, so the product batch quality risk detected by the experimenter in the early stage can be controlled.<br>3. Check the standard product administrator Cheng Wenxian, is also the first time such deviation occurred, the risk can be controlled.<br><br>1.HS-25-I three batches of sample experimental results are invalid, with the original liquid retest results issued a test report.<br>2. Training of the relevant personnel in H0-SOP-72013 Standard Management Procedure 01, emphasizing that the analysts need to check that the packaging of the standard products is in good condition before using the standard products and that the information in the label is correct.

This deviation is due to the negligence of the standard product administrator to take the wrong standard product for a while, while the inspector Wang Hao did not check the label information, resulting in the use error of the standard product and the abnormal peak time, which belongs to human error.<br>1. This deviation is caused by human error. The standard peak time is abnormal due to the use error of the standard product. The deviation map is consistent with the impurity peak of the original solution retest result, but the experimental result cannot be calculated. This experimental map is invalid and reserved for reference only. The test report is issued based on the sample original solution retest result. This deviation has no impact on the product quality evaluation.<br>2. Check the experiment of the last year of the experimenter, there is no similar error, and it is also the first deviation of using standard in the laboratory in the last two years. If the standard product is used incorrectly, it will be found in time and the risk can be controlled; therefore, the quality risk of the product batch detected by the experimenter in the early stage can be controlled.<br>3. It is the first time for Cheng Wenxian, the administrator of standard products, to find out such deviation, and the risk is controllable.<br>1. The test results of three batches of hs-25-i samples are invalid and reserved, and the test report is issued based on the retest results of the original solution.<br>2. Train relevant personnel on h0-sop-72013 standard product management procedure version 01, emphasizing that analysts need to check whether the packaging of the standard product is intact and the information in the label is correct before using the standard product.<br>