Freyr rDMS

A Compliant Document Management System.

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Overview

Freyr rDMS is a web-based, 21 CFR Part 11 compliant document management system designed to meet the specific needs of the life sciences industry. It helps organizations to manage their regulatory documents throughout their lifecycle, from creation and review to approval and archival. The system provides a secure and centralized repository for all regulatory documents, ensuring data integrity and audit readiness.

✨ Key Features

  • Document Control
  • Version Control
  • Electronic Signatures
  • Audit Trails
  • Workflow Management
  • Secure Access Controls

🎯 Key Differentiators

  • Focus on the life sciences industry
  • Cost-effective solution
  • Integration with Freyr's other regulatory solutions and services

Unique Value: Provides a compliant and cost-effective document management solution tailored for the life sciences industry.

🎯 Use Cases (4)

Managing regulatory documents for submissions Ensuring compliance with 21 CFR Part 11 Controlling SOPs and other quality documents Collaborating on document creation and review

✅ Best For

  • Used by life sciences companies to manage their regulatory and quality documents.

💡 Check With Vendor

Verify these considerations match your specific requirements:

  • Companies in non-regulated industries.

🏆 Alternatives

Veeva Vault QualityDocs MasterControl OpenText Documentum

Offers a more focused and affordable solution compared to large, enterprise-wide content management platforms.

💻 Platforms

Web

🔌 Integrations

Freyr RIM Microsoft Office

🛟 Support Options

  • ✓ Email Support
  • ✓ Phone Support
  • ✓ Dedicated Support (Available tier)

🔒 Compliance & Security

✓ GDPR ✓ ISO 27001 ✓ SSO ✓ 21 CFR Part 11 ✓ GxP

💰 Pricing

Contact for pricing

Free tier: N/A

Visit Freyr rDMS Website →