MC3 delivers integrated manufacturing services for finished medical devices. We offer services for start-up’s, IDE, CE Marking, 510K and end of life products where customer-focused project management is essential for the realization or enhancement of complex medical devices.
At MC3 we have a staff experienced in the transition, regulatory, and manufacturing of complex medical devices, including:
- Project Management
- Regulatory Planning, including IDE
- ISO 13485:2003 Guided
- Pilot and Full Scale Manufacturing
- Supply Chain Management
- Development and Manufacturing Engineering
- Verification and Validation