Instem Samarind RMS
An intelligent solution for overseeing your medical product information more effectively.
Overview
Samarind RMS is a fully integrated software application designed to mirror the processes of acquiring and maintaining a pharmaceutical product license. It emphasizes a 'data-first' approach, where information is entered once and reused for various regulatory outputs, aiming to streamline workloads and improve data quality. In late 2022, Samarind was acquired by Ennov, strengthening Ennov's position in the RIM market.
✨ Key Features
- Enter Data Once, Reuse Many Times (DRM)
- Product Lifecycle Management
- Document Management
- Office 365 Integration
- Electronic Signatures (21 CFR Part 11 Compliant)
🎯 Key Differentiators
- 'Enter Data Once, Reuse Many Times' philosophy improves efficiency and data quality
- Purpose-built to mirror regulatory processes
- Strong position in the Medical Device sector (now part of Ennov)
Unique Value: Reduces redundant data entry and improves data quality by allowing users to enter information once and reuse it across all regulatory activities.
🎯 Use Cases (4)
✅ Best For
- Centralized product data management
- Efficient lifecycle management of marketing authorizations
- Compliance with EU regulatory requirements
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Companies that require extensive, complex submission publishing features
- Organizations looking for a broad, multi-functional platform beyond core RIM
🏆 Alternatives
Offers a more fundamentally data-centric approach compared to document-centric systems, which can lead to greater efficiency.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Varies tier)
🔒 Compliance & Security
💰 Pricing
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