RAMS
RAMS serves as an innovative platform for the medical affairs sector, providing essential tools to streamline regulatory and quality management processes for medical devices and in vitro diagnostics. Users can efficiently navigate global regulations through features like product classification, Smart Builder for documentation, and automated registration tracking, ensuring compliance and facilitating expedited market access. With insights and resources from industry experts, RAMS empowers organizations to stay informed and strategically expand in the evolving healthcare landscape.
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Top RAMS Features
- Comprehensive regulatory service offerings
- Digital regulatory monitoring tools
- Human factors engineering resources
- Global medical device insights
- Automated registration tracking
- Product classification guidance
- Smart Builder documentation tool
- Regulatory Reports for market exploration
- Regulatory Watch for updates
- Registration Tracker for data control
- Process charts for strategic planning
- Global knowledge base access
- Cloud-based QMS integration
- Compliance training automation
- Industry-leading quality management system
- Multi-market regulatory insights
- Live expert training events
- Seamless device registration process
- Cross-country registration management
- Accelerated market access solutions
