SMART principles Specified: Specific, Measurable: Measurable, Attainable: achievable, Real: in line with the real situation is, Time: have temporality. Top management should provide quality objectives and measurements, they should be included in the management plan for the conduct of quality. Note: the quality objectives and customer expectations should be implemented within the time frame specified is reached. External process control 2 The second factor to consider is the degree of control of the process is shared. The share level refers to the degree of contribution of each element of the process, Handan TS16949 consultants, namely human, machine, material, method, ring, measuring the extent of sharing. Some of the outsourced process, Handan TS16949 certification consulting, organization participates, such organizations may provide raw materials or designated may arrange their own staff to do it, it might give a specific set of requirements, may provide equipment, may It will propose appropriate assessment indicators, or these possible combinations and the like. As an organization, we are also in the sharing of one or some elements of this process is not entirely fall contracted external party. There sharing and not sharing Handan TS16949, control the type and extent of the implementation is different. TS16949 system in the process of establishing and implementing common problems 07 8.2.2 Chapter prone to question 1, according to the elements of the audit, rather than the review process approach; 2, there is no audit system; 3, the audit found that no corrective action is taken; 4 Use auditors did not adequately trained; 5, no independent personnel to perform the audit; 6, documents and records are incomplete. 8.2.3 Chapter prone to Question 1, if necessary, without the application of statistical techniques; 2, the application of statistical methods ineffective; 3, ineffective application sampling systems; 4, improper exert too much control. 8.2.4 Chapter prone to question 1, to accept the lack of control materials (eg required test / inspection of the material directly to the stock); 2, assigned to the production of the material does not identify, has not been fully control; 3, the designated inspection or testing is not performed; 4, examination or test records are missing; 5, final inspection or testing is bypassed, or the company's products approval process is not executed; 6, rework the product does not completely re-examination.