New ISO 13485:2016
Introducing the New Revision of ISO 13485 Standard: Medical Devices – Quality Management System – Requirements for Regulatory Purposes.
The new edition of the ISO 13485 standard was published on 01 March 2016, concluding almost five years of intense discussion and development by experts around the world to improve and update the standard with new European requirements and other international regulatory changes, implemented since its previous revision in 2003.
ISO 13485 defines the requirements for a quality management system designed to demonstrate an organisation’s ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. Organisations complying with this standard, such as medical devices manufacturers, as well as suppliers and external parties that provide products or services to manufacturers, will be able to demonstrate compliance with regulatory requirements, manage risk, ensure best practice for quality and safety, improve processes and provide confidence to patients and users.
The new ISO 13485:2016 focuses on how companies should manage risk-based decisions related to purchasing, design, development, manufacturing, production control activities and other aspects of the quality management system.
Some of the key changes between the 2003 and 2016 version include:
Incorporation of risk-based approaches beyond product realisation. Risk is considered in the context of the safety and performance of the medical device and in meeting regulatory requirements
Increased linkage with regulatory requirements, particularly for regulatory documentation
Application to organisations throughout the life cycle and supply chain for medical devices
Harmonisation of the requirements for software validation for different software applications (QMS software, process control software, software for monitoring and measurement) in different clauses of the standard
Emphasis on appropriate infrastructure, particularly for production of sterile medical devices, and addition of requirements for validation of sterile barrier properties
Additional requirements in design and development on consideration of usability, use of standards, verification and validation planning, design transfer and design records
Emphasis on complaint handling and reporting to regulatory authorities in accordance with regulatory requirements, and consideration of post-market surveillance
Planning and documenting corrective action and preventive action, and implementing corrective action without undue delay
Organisations have until 01 March 2019 to transition from ISO 13485:2003 to ISO 13485:2016. SGS will soon provide materials, services and courses to help make the transition in the best possible conditions.
SGS is currently making arrangements with the appropriate accreditation authorities to confirm the plan to start the certification service for ISO 13485:2016 and will soon communicate accordingly.
Click here for more information on ISO 13485:2016.
For more information, contact
Lesley Pilbeam, Marketing Manager
t: 01276 697670
SGS is the world’s leading inspection, verification, testing and certification company. SGS is recognized as the global benchmark for quality and integrity. With more than 85,000 employees, SGS operates a network of over 1,800 offices and laboratories around the world.