.content:
Regulatory Content Without the Chaos
Regulatory content no longer needs to be rebuilt for every submission. freya.content uses a component-based approach — defining reusable sections, tables, or text fragments — to enable intelligent reuse across documents, products, and regions. Designed for modularity and powered by AI, it transforms fragmented content into a structured, compliant, and submission-ready single source of truth.
Real-World Use Cases
Medicinal Products
- Structured Labeling Across Markets: Author core texts and automatically generate country-specific labels with local variations.
- Component-Based Dossier Building: Break large submissions into reusable content blocks — ready for reuse in freya.submit or Dossier Builder. Manage CTD Section content as components. Assemble components to generate country specific dossier sections. Assemble the dossier sections and handle submissions all within freya fusion with Automate, Content, Submit and Dossier modules.
Medical Devices
- Modular IFU & Labeling Content Creation: Build Instructions for Use (IFUs), labels, and product manuals using reusable content blocks — ensuring consistency across product families and geographies.
- EU MDR-Compliant Document Authoring: Create content structured to meet EU MDR and IVDR format standards (e.g., SSCP, PSUR, and technical documentation) with built-in regulatory alignment.
- Cross-Product Content Reuse: Re-use validated content modules (like safety info, warnings, technical specs) across multiple product variants to reduce duplications and reviews.
Consumer
- Multimarket Pack Insert & Label Content Management: Create structured, region-specific labels and pack inserts with reusable content blocks tailored for multilingual OTC markets.
- Marketing & Regulatory Copy Harmonization: Maintain consistency between promotional messaging, claims, and regulated label content — using a single source of truth for both.
- Frequent SKU & Variant Updates: Manage high-frequency product launches and variant updates (e.g., flavor, dosage, format) through smart content versioning and reuse.
Spotlight Features
Modular Content Repository
AI/ML-driven engine breaks down documents into reusable, traceable components aligned to CTD/eCTD/SPL formats.
Smart Reuse & Versioning
Leverage intelligent matching to auto-detect duplicate content, manage updates, and track version lineage across markets.
Structured Authoring Workflows
Built-in validations and formatting logic ensure structured, compliant authoring with fewer manual errors.
Interoperable by Design
Connect freya.content with submission and archive tools for real-time updates and cross-module consistency
Template-Driven Consistency
Auto-generate regulatory documents using pre-approved templates and smart content blocks with version control.
Search, Slice & Sync
AI-powered search retrieves content by keyword or metadata; slice by region or dosage form with full traceability.
Why freya.content is Your Ideal Partner
Reuse approved content across markets to speed up submissions and ensure consistency.
Author faster with structured, compliant formats ready for CTD, eCTD, and SPL.
Push content directly into freya.submit or freya.dossierbuilder — no reformatting needed.
Ensure compliance with built-in validations that flag issues before submission.
Track every change with full visibility across authoring, approval, and archival stages.
Instantly generate region-specific documents using smart, reusable templates.
How Does freya.content Compare
| Features | freya.content | Other Content Platforms |
|---|---|---|
| Modular Content Blocks | Yes | No (Document-based) |
| Structured Authoring | Built-in | Manual |
| Submission Integration | Native with freya fusion Suite | Third-party required |
| Change Propagation Alerts | Automated | Manual effort |
| Global Content Readiness | eCTD, SPL, Labeling | Region-specific |
Take Command of Content Operations, Not Just Documents.
From draft to dossier — own your content like never before.
