BS EN ISO 19011 2026 管理体系审核指南
VIP免费
BS EN ISO 19011:2026
BSI Standards Publication
Guidelines for auditing management systems
BS EN ISO 19011:2026
BRITISHSTANDARD
National foreword
This British Standard is the UK implementation of EN ISO 19011:2026.
It is identical to ISO 1 9 0 1 1 : 2 0 2 6 . I t supersedes BS EN ISO
19011:2018, which is withdrawn.
The UK participation in its preparation was entrusted to Technical
Committee A U S / 1 , R e v i s i o n of ISO 19011.
A list of organizations represented on this committee can be obtained on
request to its committee manager.
Contractual and legal considerations
This publication has been prepared in good faith, however no
representation, warranty, assurance or undertaking (express or
implied) is or will be made, and no responsibility or liability is or will
be accepted by BSI in relation to the adequacy, accuracy, completeness,
or
reasonableness of this publication. All and any such responsibility and
liability is expressly disclaimed to the full extent permitted by the law.
This publication is provided as is, and is to be used at the
recipient's own risk.
The recipient is advised to consider seeking professional guidance with
respect to its use of this publication.
This publication is not intended to constitute a contract. Users
are responsible for its correct application.
@The British Standards Institution 2026
Published by BSI Standards Limited 2026
ISBN 9780539312911
ICS 03.100.70;03.120.10;03.120.20;13.020.10
Compliance with a British Standard cannot confer immunity from
legal obligations.
This British Standard was published under the authority of the
Standards Policy and Strategy Committee on 31 May 2026.
Amendments/corrigenda issued since publication
Date Text affected
BS EN ISO 19011:2026
EUROPEAN STANDARD
NORMEEUROPÉENNE
EUROPÄISCHE NORM
EN ISO 19011
May 2026
ICS 03.120.20 Supersedes EN ISO 19011:2018
English version
Guidelines for auditing management systems (ISO
19011:2026)
Lignes directrices pour l'audit des systèmes de
management (ISO 19011:2026)
Leitfaden zur Auditierung von Managementsystemen
(ISO 19011:2026)
This European Standard was approved by CEN on 14 May 2026.
CEN and CENELEC members are bound to comply with the CEN/CENELEC Internal Regulations, which stipulate the conditions
for giving this European Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical
References concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or
to anyCEN and CENELEC member.
This European Standard exists in three official versions (English, French, German). A version in any other language made
by translation under the responsibility of a CEN and CENELEC member into its own language and notified to the CEN-
CENELEC Management Centre has the same status as the official versions.
CEN and CENELEC members are the national standards bodies and national electrotechnical committees of Austria, Belgium,
Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland,
Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Republic ofNorth
Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Türkiye, and the United Kingdom.
CENELEC
CEN-CENELEC Management Centre:
Rue de la Science 23, B-1040 Brussels
⑥2026 CEN
/CENELEC All rights of exploitation in any formand byany means
are
reserved worldwide for CEN national Members
and for
CENELECMembers.
Ref.No.EN ISO 19011:2026E
摘要:
展开>>
收起<<
BSENISO19011:2026BSIStandardsPublicationGuidelinesforauditingmanagementsystemsBSENISO19011:2026BRITISHSTANDARDNationalforewordThisBritishStandardistheUKimplementationofENISO19011:2026.ItisidenticaltoISO19011:2026.ItsupersedesBSENISO19011:2018,whichiswithdrawn.TheUKparticipationinitspreparationwasent...
声明:如果您的权利被侵害,请联系我们的进行举报。
相关推荐
-
GB∕T 25915.2-2021 洁净室及相关受控环境 第2部分:洁净室空气粒子浓度的监测
2024-04-17 999+ -
GB∕T 25915.3-2024洁净室及相关受控环境 第3部分:检测方法VIP免费
2024-08-09 127 -
(高清)GB∕T 25915.3-2024 洁净室及相关受控环境第3部分:检测方法VIP免费
2025-08-27 999+ -
GB∕T 16886.1-2025医疗器械生物学评价 第1部分 风险管理过程中生物学安全性评价的要求和通用原则(草案稿)VIP免费
2025-09-02 831 -
GB∕T 16886.11-2021 医疗器械生物学评价 第11部分:全身毒性试验VIP免费
2025-09-02 861 -
GB∕T 191-2025 包装储运图示标志(征求意见稿)VIP免费
2025-09-29 999+ -
GB∕T 19000-2016 质量管理体系 基础和术语(高清)VIP免费
2025-10-27 999+ -
GB∕T 19001-2016 质量管理体系要求
2025-10-27 999+ -
GB∕T 16292-2025 医药工业洁净室(区)悬浮粒子的测试方法VIP免费
2025-10-29 999+ -
GB∕T 16292《医药工业洁净室(区)悬浮粒子的测试方法》2010版和2025版对比分析(逐条对比)VIP免费
2025-10-30 576
作者:雨尘yc
分类:法规规范
价格:100质量币
属性:55 页
大小:744.35KB
格式:PDF
时间:2026-06-03

