Quality management system

Management Responsibilities

£ 15.04
Management Responsibilities

Explain Management Responsibilities for the QMS including: identifying processes to include in the QMS and monitoring and measuring of those processes, determining quality goals and objectives, establishing the quality policy, communicating the quality policy and importance of meeting customer requirements, and holding Management Review.


  • SOP Management Review
  • REC Management Report
£ 15.04

Translate QM




MAN – Quality Manual

System: [Company] Quality Management System


File: "1.1 MAN Quality Manual.doc"






Version / Revision History


ISO 16949

ISO TS 16949 for Automotive Industry
ISO TS 16949 is the only quality management system standard available in the world, which has been established and controlled by International Automotive Task Force (IATF)
the members of IATF includes; ISO TS 16949 is the prerequisite to supply parts or material to most of the OEMs and TIER 1 suppliers in North America, it has also been adopted very rapidly in other parts of the world. TS 16949 was basically derived from QS 9000.

ISO 13485

Medical Device QMS

ISO 13485 is a medical device quality systems standard that supplements ISO 9001:2008. The additional requirements relate to design controls, process controls (including environmental controls), special processes, traceability, record retention, and regulatory actions, which are more critical for the medical device industry. ISO 13485 is not a product standard, but a process standard.

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