GP-12早期生产遏制程序

GP-12适用于下面要求的所有的试生产、生产、服务件和配件
Require Production Part Approval Process (PPAP) 要求提交PPAP的 Represent significant risk to the customer facility as mandated by GM GM管理 的对客户的生产厂有重要影响
建立包含以下要素的确认过程 Identify the staff person responsible for ensuring the development and implementation of the verification process. 明确保证开发和执行过程确认的责任人
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SUPPLIER RESPONSIBILITY: The supplier shall: C. Documentation: 文件Document the Pre-Launch Control Plan using the Control Plan format referenced in the AIAG Advanced Product Quality Planning and Control Plan Reference Manual or other customer approved Advanced Quality Planning reference manuals. The Pre-Launch Control Plan is not a substitute for the Production Control Plan but, is an addition to the Production Control Plan and is used to validate it 根据AIAG 的 APQP手册中控制计划表格和控制计划参考手册或其它顾客批准的APQP参考手册制定试生产控制计 划，试生产控制计划不能替代量产控制计划，它是控制计划的附加可以用来验证控制计划
1 Increased frequency/sample size as stated in the Production Control Plan.
1在产品控制计划中增加的频次和样品容量
2 Verification of packaging and label requirements – including service and accessory part requirements, which may include country of origin labels on parts. 2确认包装和标签的要求包括服务件和附件的要求，可能包括产品原产国标签 3 Verification of the effectiveness of error proofing. 确认防错的有效性 4 Immediate implementation of containment and irreversible corrective action when nonconformances are discovered in the GP-12 containment area or at the receiving location. 4如果在接受场所或在GP-12 执行的范围内发现不符合立即执行遏制措施和纠正措
1 Document additional inspections, functional testing, and dimensional checks required at the GP-12 containment station or in process check stations on the Control Plan Special Characteristics form referenced in the AIAG APQP Manual – Supplement L and reference said document in the Pre-launch Control Plan as a specific operation. GP-12 遏制站要求的额外检查、功能试验和尺寸检查要文件化，控制计划过程检查项 目特殊特性参考AIAG供应商 APQP 手册附录L，上述文件检查项目在试生产控制计划中作为特定的项 目 2 Document inspection work instruction for the GP-12 containment station to insure standardized work.GP-12 检查站要有书面的保证标准作业的检查作业指导书
3 Document evidence of execution and validation of the control plan utilizing the I-chart (GM1927-66) or other format agreed upon by the customer. The data must be readily available for review by the customer/SQE. 3要有文件证明执行和确认的控制计划运用了I-chart GM1927-66) 或顾客同意的其它格式，这些资料在 顾客或SQE评审时要易于获得 4 Document problem solving for both internal and customer quality concerns utilizing customer acceptable format; including problem description, root cause, irreversible corrective action with break points and update FMEAS and Control Plans as appropriate. The 3 x 5 Why Analysis (GM1927-84) for root cause and Read Across (GM1927-69) to apply lessons learned are to be utilized.内部和涉及到解决顾客质量问题的文件包括 问题描述、根本原因、纠正措施、FMEA和控制计划的修改要用顾客接受的格式，适时利用根本原因3 x 5 Why 分析，进行Read Across培训
The purpose of GP-12 is to: GP-12 的目的 验证供应商的量产控制计划
Validate the supplier’s production control plan
Protect our assembly and manufacturing centers and service part warehouses from quality non-conformances during critical periods 在重要时期防止我们的装配和制造中心及服务件仓库出现质量问题 Document the supplier‘s efforts to verify control of its processes during start-up, acceleration, after revisions to the manufacturing process, or when manufacturing runs are separated by 3 months or more记 录 供 应 商 在 开 始 生 产 、 加 速 生 产过 程 、生产过程变更后或生产停产三个月或以上时 ， 为 控 制 其 过程 所 做 的努力 Ensure that any quality issues that may arise are quickly identified, contained, and corrected at the supplier's location 确保任何可能产生的质量问题在供应商的生产场所尽快的得到发现、控制和 纠正 Increase involvement and visibility of supplier’s top management
增加最高管理层的参与和远见性
SUPPLIER RESPONSIBILITY: The supplier shall:供应商职责：供应商必须
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Validation Process: Establish a validation process that contains the following elements:
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பைடு நூலகம்
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SUPPLIER RESPONSIBILITY: The supplier shall:
B. Plan Development: 开发计划 Development of a Pre-Launch Control Plan which is a significant enhancement to the production control plan and also consisting of additional controls, inspections, audits, and testing to insure conformance and capability of the manufacturing process. The plan needs to consider; 试生产控制计划开发对量产控制计划有很重要得作用而且确保产品符合性和过程 制造能力附加的控制、检查、审核和试验也是根据试生产控制计划而来。试生产 控制计划必须考虑以下几个方面：
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设立GP-12 遏制站，遏制站必须设在生产末端而且不在生产线上的、单独和正常的制造过程分开的，另外的 或更有效的或可能用到过程检查站必须文件化并且有顾客或SQE批准
Identify additional inspections, testing, and dimensional checks required at the GP-12 containment station based on Key Product Characteristics (KPCs), Part Quality Characteristics (PQCs), high RPN and/or issues identified during product and process development.在GP-12检查站要识别附加的检查、试验和尺寸检验，这些检查项目来源于产 品的关键特性和产品的质量特性、高RPN值以及在产品和过程开发阶段识别的问题。 Train personnel relative to the standardized work performed at the GP-12 containment stations.培训相关人员使其满 足在GP-12 检查站岗位职责 Establish a reaction plan for single defect.建立一个针对每个缺陷反应计划 Implement an audit process of the GP-12 containment utilizing levels of management (layered audit), including site leadership, to insure conformance to the Pre-Launch Control Plan.实施GP-12审核过程，利用管理层包括现场管理 人员进行分层审核，确保符合试生产控制计划 Include subcontractor (Tier 2) in the validation process. 包括分承包方的过程确认