Medical Devices Management System
ISO 13485 is an international standard for quality management systems (QMS) specifically designed for the medical device industry. It specifies requirements for organizations involved in the design, development, production, installation, and servicing of medical devices and related services.
Key elements of ISO 13485 include:
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Management responsibility: Demonstrating leadership commitment to quality management, establishing a quality policy, and ensuring that roles, responsibilities, and authorities are defined and communicated.
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Resource management: Providing adequate resources, including personnel, infrastructure, and facilities, to support the effective implementation of the quality management system and the production of safe and effective medical devices.
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Product realization: Planning and controlling the design and development, production, and delivery of medical devices, including risk management, design verification and validation, and production process validation.
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Measurement, analysis, and improvement: Monitoring and measuring processes and products to ensure conformity to requirements, conducting internal audits and management reviews, and implementing corrective and preventive actions to address nonconformities and improve the effectiveness of the quality management system.
ISO 13485 is based on the ISO 9001 standard for quality management systems but includes additional requirements specific to the medical device industry, such as validation of processes for sterile medical devices, documentation requirements for regulatory purposes, and traceability of medical devices throughout the supply chain.
Certification to ISO 13485 demonstrates an organization’s commitment to quality management and compliance with regulatory requirements in the medical device industry. It can help medical device manufacturers and suppliers enhance their credibility, gain access to international markets, and improve customer satisfaction.