New Platform Automates Quality Management and Regulatory Compliance
The system is designed to streamline quality processes and simplify adherence to ISO, FDA, and EU MDR requirements for regulated industries.
The system is designed to streamline quality processes and simplify adherence to ISO, FDA, and EU MDR requirements for regulated industries.
Effective post-market surveillance depends on HTM teams to bridge the gap between regulatory oversight and real-world performance.
The FDA-cleared system uses artificial intelligence to create interactive 3D models from standard medical scans for preoperative planning and intraoperative guidance.
Ongoing innovation is driving a new generation of dialysis systems designed to enhance patient safety and operational efficiency.