Freyr iReady

A modular, data-driven RIM system built on ISO IDMP standards.

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Overview

Freyr's RIM solution is a modular, well-structured, product data-driven system built from the ground up on ISO IDMP standards. It assists users in managing information from product registrations and marketing authorization lifecycles to health authority interactions and correspondence.

✨ Key Features

  • Product Registration Tracking
  • Marketing Authorization Lifecycle Management
  • Regulatory Document Management
  • Health Authority Interaction Tracking
  • Built on ISO IDMP standards

🎯 Key Differentiators

  • Built from the ground up on ISO IDMP standards
  • Combines software with extensive regulatory services and consulting
  • Modular approach allows for flexibility

Unique Value: Provides a future-proof RIM system foundationally built on IDMP standards, combined with deep regulatory expertise to ensure compliance.

🎯 Use Cases (4)

Managing global product registrations Ensuring compliance with IDMP standards Tracking the entire lifecycle of marketing authorizations Centralizing regulatory documents and correspondence

✅ Best For

  • IDMP-compliant product data management
  • End-to-end lifecycle tracking for pharmaceutical products
  • Global regulatory information management

💡 Check With Vendor

Verify these considerations match your specific requirements:

  • Companies not focused on IDMP compliance
  • Organizations looking for a simple, non-modular system

🏆 Alternatives

Veeva Vault RIM ArisGlobal LifeSphere RIM EXTEDO RIM ONE

Offers a more specialized focus on IDMP and structured data management than many general-purpose RIM systems.

💻 Platforms

Web API

🔌 Integrations

Freyr Publishing Tools Freyr Labeling Suite API

🛟 Support Options

  • ✓ Email Support
  • ✓ Live Chat
  • ✓ Phone Support
  • ✓ Dedicated Support (Varies tier)

🔒 Compliance & Security

✓ GDPR ✓ ISO 27001 ✓ SSO ✓ 21 CFR Part 11 ✓ GxP ✓ ISO 9001

💰 Pricing

Contact for pricing
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