Click-N-Manage allows you to describe the procedures necessary to comply with the requirements of Regulation (EU) 2017/745 on medical devices.
Some examples:
- Risk-based approach
- Control of outsourced products / services
- Validation of software applications
- Quality Manual
- Technical file of the medical device
- Management of sensitive medical data
- Management of hygiene rules and contamination control
- Communication with authorities
- Traceability of design decisions
- Product identification
- Management of market feedback
- Management of non-conformities after delivery
- …