6.3.23评价/测量技术此栏标明所采用的计量系统，包括测量产品/流程

6.3.23 Evaluation/Measurement Technology This column indicates the measurement system used, including the measuring tools, fixtures, and/or test devices required to measure the product/process/manufacturing device. The linearity, reproducibility, stability and accuracy analysis of the measurement system should be completed in advance to make the measurement system credible, and these analyses must be continued after improvements are made. <br>6.3.24 Sample size/frequency When sampling is required, list the corresponding sample size and sampling frequency. <br>6.3.25 Control method This column contains a brief description of how to control the operation, including the procedure number used if necessary. The controls used should be based on an effective analysis of the process. The control method depends on the type of process that exists, and can be used (but not limited to) statistical process control, inspection, counting data, error prevention (automatic/non-automatic), and sampling plan to control the operation. The description of the control plan (QC engineering drawing) should reflect the planning and strategy implemented in the production process. If a complex control program is used, the plan needs to refer to the specific identifying name or number of the program file. In order to achieve the effectiveness of process control, the control method should be continuously evaluated. For example, when there is a major change in the process or process capability, the control method should be reviewed again. <br>6.3.26 The reaction plan specifies the corrective measures required to avoid the production of substandard products or the operation out of control. These measures are usually to clarify the responsibilities of the personnel most closely related to the process (operators, adjustment personnel or management personnel) in the plan. To specify. All preventive measures should be documented. In all cases, suspicious products and substandard products must be clearly marked and isolated, and handled by the responsible person designated in the response plan. This column can also use a dedicated reaction plan number to indicate and determine the person in charge of the reaction plan. <br>6.4 Review and update of the control plan (QC engineering drawing) <br>6.4.1 When the following situations occur, if necessary, the control plan (QC engineering drawing) must be reviewed and updated <br>----- product changes <br>----- process Change <br>----- Unstable process <br>----- Insufficient process capability <br>----- Revision of inspection method and frequency

6.3.23 Evaluation/Measurement Technology This column indicates the measurement system used, including the measuring of the gaugs, fixtures, and/or test devices required for the product/process/manufacturing device. The linear, reproducible, stability, and accuracy analyses of the measurement system should be done in advance to make the measurement system credible, and these analyses need to continue after improvements have been made.<br>6.3.24 Sample size/frequency When sampling is required, list the corresponding sample size and sampling frequency.<br>6.3.25 Control Method This column contains a brief description of how to control the operation and, if necessary, the program number used. The controls used should be based on an effective analysis of the process. Depending on the type of process that exists, control operations can be controlled (but not limited to) statistical process control, inspection, counting data, error-proofing (auto/non-automatic), sampling schedule, etc. The description of the control plan (QC drawing) should be reflected in the planning and strategy implemented during the production process. If a complex control program is used, the plan refers to the specific identification name or number of the program file. In order to achieve the effectiveness of process control, control methods should be continuously evaluated, such as when significant changes in process or process capability occur, and control methods should be re-evaluated.<br>6.3.26 The response plan sets out the corrective actions required to avoid the production of substandard products or out-of-control operations, which are usually clearly identified in the plan the responsibilities of the person most closely related to the operation (operator, adjuster or manager). Precautions should be documented in all cases, suspect and non-conforming products must be clearly marked and isolated and handled by the responsible person designated in the response plan. This column can also represent and identify those responsible for the response plan using a dedicated response plan number.<br>6.4 Review and update of the Control Plan (QC Drawings).<br>6.4.1 Control plans must be reviewed and updated if necessary (QC drawings)<br>----- product changes.<br>----- process changes.<br>----- process is unstable.<br>----- process capability is insufficient.<br>----- the inspection method, frequency, etc.

6.3.23 evaluation / measurement technology this column indicates the measurement system used, including the measuring tools, fixtures, and / or test devices used to measure the product / process / manufacturing device. The linearity, reproducibility, stability and accuracy analysis of the measurement system should be completed in advance to make the measurement system credible, and these analyses should be continued after the improvement.<br>6.3.24 sample size / frequency when sampling is required, list the corresponding sample number and sampling frequency<br>6.3.25 control method this column contains a brief description of how to control the operation, including the procedure number to be used if necessary. The control used should be based on an effective analysis of the process. The control method depends on the type of process that exists, and the operation can be controlled by (but not limited to) statistical process control, inspection, counting data, error proofing (automatic / non automatic) and sampling plan. The description of the control plan (QC engineering drawing) should reflect the planning and strategy implemented in the production process. If a complex control program is used, the plan needs to refer to the specific identification name or number of the program document, and the specific identification name or number of the program document. In order to achieve the effectiveness of process control, the control method should be continuously evaluated. For example, when there is a significant change in process or process capability, the control method should be reviewed again.<br>6.3.26 the response plan specifies the corrective measures needed to avoid the production of unqualified products or out of control operation. These measures usually specify the responsibilities of the personnel most closely related to the process (operators, adjustment personnel or management personnel) in the plan. All preventive measures shall be documented. In all cases, suspicious products and unqualified products must be clearly marked and isolated, and handled by the person in charge designated in the response plan. The special response plan number can also be used to indicate and determine the person in charge of the response plan.<br>6.4 review and update of control plan (QC engineering drawing)<br>6.4.1 the control plan (QC engineering drawing) must be reviewed and updated if necessary in the following situations<br>-----Product change<br>-----Process change<br>-----The process is unstable<br>-----Insufficient process capability<br>-----Revision of test method, frequency, etc<br>