IATF16949認(rèn)證要求修訂認(rèn)可解釋SI12-13
IATF16949認(rèn)證要求修訂認(rèn)可解釋SI12-5.1.1.2 Process effectiveness and efficiency過(guò)程有效性和效率
Top management shall review the product realization processes effectiveness and efficiency of the quality management system and support processes to evaluate and improve their effectiveness and efficiency the organization’s quality management system. The results of the process review activities shall be included as input to the management review (see Section 9.3.2.1.).
高層管理人員應(yīng)審查 產(chǎn)品實(shí)現(xiàn)過(guò)程和質(zhì)量管理體系的有效性和效率，并支持過(guò)程以評(píng)估和提高組織質(zhì)量管理體系的有效性和效率 。過(guò)程審查活動(dòng)的結(jié)果應(yīng)作為管理審查的輸入(見(jiàn)第9.3.2.1節(jié))。
Rationale for change改變?cè)?
Clarified that not every process requires an efficiency measure. The organization needs to determine which processes require efficiency measures within their quality management system. Additionally, the organization’s problem-solving processes need to have an effectiveness review conducted by the organization’s management.
闡明并不是每個(gè)過(guò)程都需要效率測(cè)度。組織需要確定在他們的質(zhì)量管理體系中哪些過(guò)程需要效率測(cè)度。此外，組織的問(wèn)題解決過(guò)程需要由組織的管理人員進(jìn)行有效性審查。
IATF16949認(rèn)證要求修訂認(rèn)可解釋SI13-9.3.2.1 Management review inputs – supplemental管理評(píng)審輸入-補(bǔ)充
Input to management review shall include:
a) cost of poor quality (cost of internal and external nonconformance);
b) measures of process effectiveness;
c) measures of process efficiency for product realization processes, as applicable;
d) product conformance;
e) assessments of manufacturing feasibility made for changes to existing operations and for new facilities or new product (see Section 7.1.3.1);
f) customer satisfaction (see ISO 9001, Section 9.1.2);
g) review of performance against maintenance objectives;
h) warranty performance (where applicable);
i) review of customer scorecards (where applicable);
j) identification of potential field failures identified through risk analysis (such as FMEA);
k) actual field failures and their impact on safety or the environment.
管理評(píng)審的輸入應(yīng)包括:
a) 不良質(zhì)量成本 (內(nèi)部和外部不符合的成本);
b) 過(guò)程有效性的測(cè)量;
c) 產(chǎn)品實(shí)現(xiàn)過(guò)程的過(guò)程效率測(cè)度, 如適用;
d) 產(chǎn)品符合性;
e) 對(duì)變更現(xiàn)有業(yè)務(wù)和新設(shè)施或新產(chǎn)品的制造可行性進(jìn)行評(píng)估(見(jiàn)第7.1.3.1節(jié));;
f) 客戶(hù)滿(mǎn)意度(見(jiàn)ISO 9001，第9.1.2節(jié));;
g) 根據(jù)維護(hù)目標(biāo)審查績(jī)效;
h) 保修績(jī)效 (如適用);
i) 審查客戶(hù)記分卡 (如適用);
j) 通過(guò)風(fēng)險(xiǎn)分析(如FMEA)識(shí)別潛在的現(xiàn)場(chǎng)故障;
k) 實(shí)際現(xiàn)場(chǎng)故障及其對(duì)安全或環(huán)境的影響。
Rationale for change改變?cè)?
Clarified that not every process requires an efficiency measure. The organization needs to determine which processes require efficiency measures within their quality management system.
闡明并不是每個(gè)過(guò)程都需要效率測(cè)度。組織需要確定在他們的質(zhì)量管理體系中哪些過(guò)程需要效率測(cè)度。
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