Quality_Jiangsu tiankang biotechnology co., LTD

Serial number	Process flow	Responsibility department			Demand note
Serial number	Process flow	MR	AT	CD	Demand note
1	Annual internal audit plan 　 Internal audit implementation plan 　 Internal audit to prepare 　 Implementation of internal audit Internal audit report Non-conformance correction Correct verification Shut down	R	P	P	. Must include all elements specified in all shifts and quality systems. . Internal quality system audit is generally twice a year. . The qualification of product audit, process audit and internal quality system personnel shall be referred to the "provisions on the qualification of internal quality audit personnel". During the internal audit, internal audit personnel must be guaranteed to have no direct responsibility relationship with the audited department. . When there is a major change in the architecture or a major nonconformity, or customer complaint, the management representative may organize a temporary local internal audit. . The audit leader and members of the audit team selected by the management representative about two weeks before each audit shall prepare the internal quality system audit implementation plan according to the annual plan. The implementation plan shall include all the processes, activities and shifts related to quality management. . The audit leader shall take the lead in formulating the system audit checklist. . The audit team follows:. The grading criteria specified in the criteria are graded. 　. After each audit, the audit leader shall summarize the audit and prepare the internal quality system audit report. . All nonconformities in the audit nonconformities report shall have sufficient evidence and be signed and confirmed by the person in charge of the audit department, which shall immediately propose corrective measures and determine the time for the completion of the measures. The auditor shall verify the effectiveness of the corrective measures and conclude the case within the fifth working day after the specified completion time. . If the verified corrective measures are invalid or the effect is not obvious, the auditor shall record the facts, and the audit leader shall inform the audited cross-department to re-formulate the audit measures and determine the date of completion. . The conclusion of internal audit will be one of the important contents of management review. . The method of product audit and process audit shall refer to product quality audit specification and process audit specification respectively.
2		P
3		P
4		P
5		P
6		P
7		P
8		R
R - - - is responsible for P - to participate in I --, notify		MR-- management representative The AT - team conducted a process-based CD-- related departments

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Quality