ISO 13485 - Medical Device QMS
ISO 13485 is a certification intended for organizations that provide medical devices. The standard puts an emphasis on regulatory requirements, custom requirements, risk management, and maintaining effective processes such as safe design, manufacture, and distribution of medical devices.
Benefits:
- Improves customer confidence and trust.
- Efficient processes, documentation and streamlined operations.
- Better supplier relationship manager.
- Access to a wider and global market.