Structured. Governed. Built for What’s Next.
Pharma teams must deliver complex, compliant content faster and across more markets—but static documents still slow them down.
Even with RIM and publishing tools, content trapped in outdated formats causes version issues and rework.
Docuvera changes that.
We combine structured authoring with practical AI to streamline content creation, reuse, and submission. Modular components and governed workflows scale with your needs—improving consistency without sacrificing control.
At Docuvera, AI reduces friction without replacing expertise. It detects variants, normalizes terms, recommends reuse, accelerates initial drafts, and classifies metadata—all under human review.
Structured Content Done Right.
Docuvera doesn’t just support structured content—it enforces it with rigor.
Content is broken into governed, metadata-rich components—each tagged for traceability, region, indication, use case, and approval. Nothing is orphaned. Every unit is linked, owned, and fully auditable.
Built-In Control
- The platform ensures that every component has:
- Defined owners and version history
- Regulatory and functional context (e.g., which SmPC or CCDS it’s tied to)
- Approval status and audit trail across its entire lifecycle
- This transforms compliance from a last-minute checklist into a built-in feature of how content is created and maintained.
Efficient Authoring Without Oversight Loss
Docuvera provides templated authoring environments aligned to global health authority standards. Writers are guided by compliance-ready structures, while reviewers gain clear visibility into what changed, why, and where it’s reused.
There’s no need to “start from scratch,” no copy-pasting across modules, and no black-box automation that risks quality or compliance.
One Source, Multiple Outputs
Structured components can be assembled into:
- Regulatory submissions
- Global labeling artifacts
- Safety and clinical content
- Patient communication documents
Each output is derived from the same set of governed building blocks—ensuring consistency across formats, geographies, and channels without duplicating effort.
Designed for Real-World Life Sciences Workflows.
Docuvera supports a full range of structured content use cases:
- Labeling: CCDS, SmPCs, USPIs, and patient leaflets
- Regulatory: Module 1 and 2 documents, variation responses, risk management content
- Clinical & Safety: Narratives, periodic safety updates, CSRs
- Global Documentation: Master templates, territory-specific labeling, harmonized summaries
Why Structured Content and AI Work Better Together
The intersection of modular content and targeted AI produces measurable results:
- Content creation time drops significantly due to reusable building blocks
- Updates become traceable and scalable, not error-prone one-offs
- Teams can generate variations of first draft content while typing it back to a single, trusted source
- Compliance improves as terminology, structure, and governance are standardized
Structured content enables scale. AI accelerates the work within it. Docuvera brings them together in a platform that’s purpose-built for pharma—not adapted from marketing or general-purpose writing tools.
