The quality assurance of medical devices is vital to ensure compliance with regulatory requirements and requirements of customers. These issues are covered by standard ISO 13485. ISO 13485:2016 will help you detect critical points and set up and monitor individual processes to ensure the continuous quality of medical devices, including their design, production, assembly and maintenance. ISO 13485 is recommended to organizations whose activities involve medical devices in any stage of their supply chain.
Requirements:
- Implementation of extensive requirements for medical facilities.
- Definition and monitoring of relevant processes in view of legal requirements.
- Validation of processes.
- Assuring traceability of products.
Benefits:
- Assuring the necessary quality of medical devices in the entire supply chain.
- Improved risk detection and better solutions.
- Improved competitiveness.
- Greater trust of your clients.
- Compliance with all legal and regulatory requirements.
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