Regislate
REGISLATE® revolutionizes registration management for medical devices and IVDs, offering users tailored submission requirements by country. It enables real-time tracking of milestones and progress, simplifying initial registrations, renewals, and amendments. With infographic data and collaboration tools, users efficiently prepare and monitor compliance documents across 140+ countries, streamlining global market access.
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Top Regislate Features
- Device-specific submission requirements
- Country-specific registration processes
- Real-time milestone tracking
- Estimated and actual completion dates
- Infographic project monitoring
- Proprietary performance indicators
- GR-MAP registration tracking
- Collaboration tools for submissions
- Real-time progress reports
- Market access readiness index
- Automated registration life cycle
- Multi-country submission management
- Quick onboarding process
- Compatibility with 140+ countries
- Simplified compliance information access
- Streamlined amendment and renewal tracking
- Centralized document management
- User-friendly interface
- Efficient market access strategies
- Enhanced regulatory compliance support
