Veeva Vault RIM Suite
Unified RIM to streamline global regulatory processes.
Overview
The Veeva Vault RIM Suite provides unified regulatory information management (RIM) capabilities on a single cloud platform. It includes applications for submission document management, product registration management, health authority correspondence, and submission archiving, designed to improve visibility, data quality, and agility for life sciences companies.
✨ Key Features
- Submission Document Management
- Product Registration Tracking
- Health Authority Correspondence Management
- Submission Publishing and Archiving
- Regulatory Intelligence Data
- Dossier Management
🎯 Key Differentiators
- Unified suite on a single cloud platform
- Deep specialization in life sciences
- Pre-built integrations with other Veeva Vault applications
Unique Value: Provides a single source of truth for regulatory information across the enterprise, accelerating time-to-market and improving compliance.
🎯 Use Cases (4)
✅ Best For
- Global submission coordination for Pharma & Biotech
- Medical Device MDR/IVDR compliance
- Centralized dossier planning and management
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Small startups with very limited budgets
- Companies outside the life sciences industry
🏆 Alternatives
Offers a more integrated and comprehensive suite of applications compared to point solutions, reducing the need for complex integrations.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Live Chat
- ✓ Phone Support
- ✓ Dedicated Support (Enterprise tier)
🔒 Compliance & Security
💰 Pricing
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