Preserve originals and the effective source structure
Know what every document is, what it supports, and where it came from.
Turn structured submissions, dossier archives, and connected repositories into one searchable, governed evidence map for downstream regulatory work.
01Effective source structure
02Document-level intelligence
03Controlled evidence retrieval
Real Artivex interface—not a conceptual diagram.

Turn every source dossier into usable regulatory intelligence.
Artivex preserves the submitted source, resolves its effective hierarchy, inventories every file, and makes evidence searchable by regulatory purpose—not merely by filename or folder.
Move the work forward
without losing control.
Build a complete, searchable dossier document map
Understand what each file is and what it supports
Retrieve evidence by requirement, purpose and product context
A controlled path from input to approved result.
The workflow remains explicit, reviewable and connected to the product record.
Import
Bring in a structured dossier, submission sequence, archive, or connected repository.
Normalize
Preserve the source while resolving the effective document hierarchy.
Understand
Classify purpose, evidence type, product context, and likely placement.
Control
Review exceptions and publish a reusable approved source map.
Fast enough to matter.
Controlled enough to trust.
Artivex combines automation with the evidence, review and operational context pharmaceutical teams need.
Originals preserved
Source files remain intact and retrievable.
Structured intelligence
Every document receives usable regulatory context.
Human review
Ambiguities surface instead of disappearing.
Reusable source
One normalized map powers downstream workflows.
Bring one product.
We’ll show you the system.
Walk through the source evidence, workflow and destination that matter most to your team.
Book a private demo