ISO 13485 – Medical Devices Management Systems Certification
ISO 13485 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide Medical Devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services.
Benefits of ISO 13485 certification to your organization:
- Global Recognition
- Improved legal and regulatory or contractual requirements compliance
- ISO 13485 Medical Devices Quality Management System (QMS) is very close to the Food and Drug Administration’s (FDA) QSR standards.
- Assistance in monitoring supply chain effectiveness
- Increased profit margins
- Improved product safety
- Increased Efficiency
- Proactive error detection and prevention
- Cost Savings
- More Effective Risk Management
- Increased likelihood of meeting Customer Requirements
Benefits of ISO 13485 certification to your customers:
- Quality ensured medical devices
- Safe and effective medical devices
- Lower skepticism and increased confidence for end-customer
- Boost of loyal customers and potential customers
- Increased profit margins
ISO 13485 certification
ISO 13485 certification (also known as “registration”) is a third-party audit performed by a certification body who, upon verification that an organization is in compliance with the requirements of ISO 13485, will issue anISO 13485 certificate. This certification is then maintained through regularly scheduled annual surveillance audits by the registrar, with re-certification of the Quality Management System performed on a triennial basis.