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The ISO 9000 family consists of the world's best known standard for quality management systems (QMS), ISO 9001, along with a set of supporting standards on quality management, all published by ISO/TC 176 and its subcommittees.

ISO 9001 provides a quality management framework that can apply to organizations of any size or sector. ISO 13485, on the other hand, has been developed specifically for the medical device industry with a focus on regulatory compliance.

At ISO, we develop International Standards, such as ISO 9001 and ISO 14001. ISO's Committee on Conformity Assessment (CASCO) has produced a number of standards related to the certification process, which are used by certification bodies.

ISO 19011 is an international standard that provides guidelines for auditing management systems, including quality management systems (ISO 9001) and environmental management systems (ISO 14001). It outlines the principles of auditing, managing audit programs, and conducting management system audits.

ISO 19011:2011 provides guidance on auditing management systems, including the principles of auditing, managing an audit programme and conducting management system audits, as well as guidance on the evaluation of competence of individuals involved in the audit process, including the person managing the audit programme, auditors and audit teams.

L'ISO 19011:2011 fournit des lignes directrices sur l'audit de systèmes de management, comprenant les principes de l'audit, le management d'un programme d'audit et la réalisation d'audits de systèmes de management.

meet the ISO 9001 requirements in your organization. ISO 9001 defines what you should do to consistently provide product that meets customer expectations and applicable statutory and regulatory requirements. In addition, you will seek to enhance customer satisfaction by continual improvement of your quality management system.

ISO 19900:2019 Petroleum and natural gas industries — General requirements for offshore structures

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