Regulatory Affairs
Regulatory Affairs consulting for medical devices is one of the key services provided by 8C Healthcare. We provide regulatory services in all the major medial device markets including US, EU, Canada, Australia and India. The important topics that we cover under this vertical are
- Technical File Compilation
- Regulatory Intelligence Reports
- Design Control Implementation
- DHF Remediation
- Risk Management File preparation
- Usability Engineering Documentation
- Clinical Evaluation Report Compilation
We provide regulatory consulting services pertaining to the following countries
Europe
Regulatory Affairs
Europe
India
Regulatory Affairs
India
Canada
Regulatory Affairs
Canada
Australia
Regulatory Affairs
Australia