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Generis CARA

The data and content management platform for regulated industries.

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Overview

Generis CARA is a comprehensive platform that provides a single information management system for regulatory, quality, clinical, safety, and legal teams. It offers a range of applications, including a RIM solution, that help organizations to manage their content and data in a compliant and efficient manner. The platform is highly configurable and can be tailored to the specific needs of each organization.

✨ Key Features

  • Regulatory Information Management
  • Quality Management
  • Clinical Document Management
  • Safety and Pharmacovigilance
  • Enterprise Content Management
  • Low-code/No-code configuration

🎯 Key Differentiators

  • Unified platform for multiple business functions
  • Highly configurable with a low-code/no-code approach
  • Strong focus on user experience

Unique Value: Provides a single, unified platform for managing all regulated content and data, breaking down silos between departments.

🎯 Use Cases (4)

Managing regulatory submissions and registrations Controlling quality documents and processes Managing clinical trial documentation Ensuring compliance across the enterprise

✅ Best For

  • Used by life sciences companies to manage their regulated content and data.

💡 Check With Vendor

Verify these considerations match your specific requirements:

  • Organizations looking for a simple, point solution for a single regulatory function.

🏆 Alternatives

Veeva OpenText Documentum MasterControl

Offers greater flexibility and a more modern user experience compared to legacy enterprise content management systems.

💻 Platforms

Web API

🔌 Integrations

Microsoft Office 365 SAP Veeva Vault

🛟 Support Options

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

🔒 Compliance & Security

✓ GDPR ✓ SSO ✓ 21 CFR Part 11 ✓ GxP

💰 Pricing

Contact for pricing

Free tier: N/A

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