ISO 13485:2016 (Quality Management System- Requirements for regulatory purposes for medical device manufacturers)           
ISO 13485 is an ISO standard, published in 2016, that represents the requirements for a comprehensive management system for the design and manufacture of medical devices.All requirements of this International Standard are specific to organizations providing medical devices, regardless of the type or size of the organization.This standard supersedes earlier documents such as EN 46001 and EN 46002 (both 1997),the ISO 13485 published in 2003 and 2012. ISO 13485 is a quality system standard designed specifically for medical device companies. The standard is applied by most Class II and III (plus Class IV in Canada) medical device manufacturers to meet the quality system requirements of Europe, Canada, Australia, Japan and other parts of the world.
Compliance with ISO 13485 is often seen as the first step in achieving compliance with ISO 13485:2016, based on the ISO 9001:2015 process model,  suggests that the application and management of a system of processes is an effective way to ensure good quality management.All requirements of this International Standard are specific to organizations providing Medical Devices,regardless of the type or size of the organization.
13485 are in part designed to produce a management system that facilitates compliance to the requirements of customers and pre-eminently various global regulators. While being certified to 13485 does not fulfill the requirements of either the FDA or foreign regulators, the certification aligns an organization's management system to the requirements of the FDA's Quality System Regulation (QSR) requirements as well as many other regulatory requirements found throughout the world. Therefore, 13485 certification serves to create a management system that can be thought of as a framework on which to build compliance to various regulatory and customer requirements.
The ISO 13485 standard supplements ISO 9001 and has many of the same requirements. However, there are additional requirements for process control, design control, retention of records, accountability, traceability, customer satisfaction and more. Individual countries such as Canada and Japan have additional requirements necessary to meet their specific regulations. ISO 13485 certification is not accepted by the US FDA, although it shares many of the same characteristics as FDA Good Manufacturing Practice (GMP).

Though based on ISO 9001, 13485 remove 9001's emphasis on continual improvement and customer satisfaction. In its place is an emphasis on meeting regulatory as well as customer requirements, risk management and maintaining effective processes, namely the processes specific to the safe design, manufacture and distribution of medical devices.
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