イベント概要
This course provides trainees with the practical knowledge and skills necessary to plan, conduct and report an internal audit under ISO 9001:2015 quality management system (QMS) Trainees will learn how to audit based on ISO 9001 requirements after understanding the auditing protocols and practice based on ISO 19011.
Why attend?
Who should attend?
Management representatives, Quality/EHS managers, Engineers, Executives, and other personnel involved in Quality matters.
For any questions relating to the training or certification, please feel free to contact:
Lillian Ching
Business Development
Academy & Life Care, Asia Pacific
lillian.ching@tuv.com
Tel: +65 6562 8750 Ext. 3326
Mobile No. +65 9728 0122
Andrew Lim
Account Manager, Systems
andrew.lim@tuv.com
Tel: +65 6562 8750 ext. 3317
Mobile: +65 9755 2588
Why attend?
- Be familiar with the revised structure of the standards ISO 9001
- Understand the potential impact of the revised standard on Quality Management System being audited
- Be able to make informed decisions about adaption of the revised standard to your current Quality Management System
- Understand the options of implementations of the revised standards
- Understand the mechanism of internal auditing
Who should attend?
Management representatives, Quality/EHS managers, Engineers, Executives, and other personnel involved in Quality matters.
For any questions relating to the training or certification, please feel free to contact:
Lillian Ching
Business Development
Academy & Life Care, Asia Pacific
lillian.ching@tuv.com
Tel: +65 6562 8750 Ext. 3326
Mobile No. +65 9728 0122
Andrew Lim
Account Manager, Systems
andrew.lim@tuv.com
Tel: +65 6562 8750 ext. 3317
Mobile: +65 9755 2588
終了したイベント
-
2018/10/22(月) (開始時間未定) (GMT+08:00)
Data Protection Officer (TÜV) Including the EU General Data Protection Regulation (GDPR) 22 – 26 October 2018
-
2018/09/24(月) (開始時間未定) (GMT+08:00)
Data Protection Officer (TÜV) Including the EU General Data Protection Regulation (GDPR) 24 – 28 September 2018
-
2018/08/30(木) (開始時間未定) (GMT+08:00)
Medical Device Software: Compliance with International Regulations IEC 60601-1 and IEC 62304