Ennov RIM

Unified Regulatory Information Management.

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Overview

Ennov RIM is a part of the Ennov platform for life sciences, providing a unified solution for managing regulatory information. It helps organizations to streamline their regulatory processes, from submission planning and tracking to registration management and health authority correspondence. The platform is highly configurable and can be adapted to meet the specific needs of different organizations.

✨ Key Features

  • Product and Registration Tracking
  • Submission Planning and Management
  • Health Authority Correspondence
  • Labeling Management
  • IDMP and XEVMPD Compliance
  • Configurable Workflows

🎯 Key Differentiators

  • Unified platform with QMS and clinical solutions
  • Highly configurable to meet specific needs
  • Strong presence in Europe

Unique Value: Offers a highly configurable and unified platform for managing regulatory, quality, and clinical information.

🎯 Use Cases (4)

Managing global product portfolios Tracking regulatory submissions and approvals Ensuring compliance with international regulations Managing product labeling and variations

✅ Best For

  • Used by a range of life sciences companies to manage their regulatory information.

💡 Check With Vendor

Verify these considerations match your specific requirements:

  • Organizations looking for a very simple, out-of-the-box solution may find the configurability adds complexity.

🏆 Alternatives

Veeva Vault RIM IQVIA RIM Smart MasterControl

Provides greater flexibility and customization options compared to more rigid, out-of-the-box solutions.

💻 Platforms

Web API

🔌 Integrations

Ennov QMS Ennov Clinical Microsoft Office Documentum

🛟 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 Ennov RIM Website →