One platform. The complete ePI lifecycle.
NASHRA consolidates every stage of your digital leaflet workflow into a single, cohesive pipeline — from raw document ingestion to certified FHIR R5 submission. No switching tools. No data loss.
The NASHRA pipeline, live.
Watch data flow through each stage — or click any step to explore it. The pipeline advances automatically.
Ingest Source Material
Drag-and-drop raw regulatory files — PDFs, Word documents, legacy XMLs. Or use the Unified XML Import Wizard to batch-import multi-MPD structures and auto-link inline PDFs in one pass.
What happens here
- Drag-and-drop PDF / DOCX / XML
- Unified XML Import Wizard
- Multi-MPD batch passthrough
- Inline PDF auto-linking
Enterprise-grade portfolio namespacing.
NASHRA structures your entire pharmaceutical portfolio under clean, auditable corporate namespaces — from top-level MAH down to individual version diffs.
Marketing Authorization Holders (MAHs)
Manage multiple manufacturing entities, regional subsidiaries, or corporate divisions from a unified administrator ledger — with row-level access controls per MAH.
Dossier Collections with Safety Gates
Group leaflets by molecule or therapeutic project. Dossiers enforce MAH-scoped uniqueness constraints and a deliberate 3-second hold-to-delete mechanism to prevent catastrophic data loss.
FHIR R5 Bidirectional Global Linking
Connect parent documents with regional translations. The engine groups document families automatically, blocks circular connections, and embeds strict <relatesTo> XML definitions in every export.
Circular linking (child → parent → child) is blocked at the engine level.
Ready to automate your ePI packaging?
Book a platform walkthrough and see the full workflow — from PDF ingestion to certified FHIR R5 submission — in 30 minutes.