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Oushvaa™ · the reference layer

The reference layer for pharmaceutical decisions.

Every drug, device, biologic, and procurement transaction — linked into one canonical record, across every regulator, and answerable in plain language. The data was always public. Oushvaa is the first to link it. India-first, structurally global.

It cites, or it does not answer.

597,711 canonical drug records 75.5M FAERS drug-event records 5.09M device records 66,252 canonical companies 20 regulators
The problem

Public, but unusable.

The facts exist — drug approvals in one regulator's portal, price ceilings in another, adverse-event reports in a third, device recalls in a fourth — across the FDA, EMA, CDSCO, NPPA, and dozens more. Each speaks its own format, its own identifiers, its own language. So the people who need answers do one of two things.

Option one

Reconstruct it by hand

Analysts with thirty browser tabs, spreadsheets, and a two-week turnaround for a question that should take thirty seconds.

Option two

Buy a Western premium tool

Deep, but India-blind — and priced for the global top-100, out of reach for the Indian teams, hospitals, and institutions who need it most.

The gap is not a missing dataset. It is that nobody has linked the datasets that already exist. Aggregation is cheap. Linking is the hard, durable thing.

The moat

One canonical graph. The graph is the company.

A single company resolves to its drugs, its biologics, its devices, and its procurement footprint — across India's national registries and the global regulators. The same molecule, the same manufacturer, the same device, under a different name in every portal — canonicalized to one stable ID. That cross-walk takes years to build and cannot be backfilled.

canonical company DrugIQ BiologicsIQ MedevIQ Procure OushIQ synthesises across the intelligence rails →
66,252
Canonical companies in the entity graph — the backbone for resolving one company across every rail.
20
Regulators with approval data, India-first and crosswalked to FDA, EMA & WHO.
Linked
Not aggregated — linked. The cross-walk is the asset, and it compounds with every rail.
The platform

One graph. Five surfaces.

The graph is the company; the five products are how different people reach into it. Each links its domain — across every authority — into one queryable, citable database.

Synthesis

OushIQ

The synthesis layer that reads across the three rails to answer questions no single rail can. One question across drug, biologic, and device data — traced to the source record. Grounded, not generated: it cites, or it does not answer. Private hospital data never enters OushIQ.

Visit oushiq.ai →
What the graph unlocks

Questions no single database can answer.

Because one company, one molecule, one device resolves to a single ID across every rail, the platform answers the questions that live between the silos — the ones that used to take thirty tabs and a fortnight.

Which drugs carry a QT-prolongation safety signal — and come from a manufacturer with a flagged cardiac device?
FAERS safety signals joined to device records through the shared canonical company ID.
DrugIQMedevIQ
For this biosimilar, what is the reference product's India price, safety profile, and regulatory status?
Originator↔biosimilar linkage, resolved to NPPA pricing and pharmacovigilance.
BiologicsIQDrugIQ
Before we award this tender, do any of the listed devices have open recalls or warning letters?
Procurement checked against live device intelligence at the moment of decision.
ProcureMedevIQ
Which companies appear across all three rails — as a drug maker, a device maker, and a biologic sponsor?
One canonical company, resolved across every domain it operates in.
DrugIQMedevIQBiologicsIQ
The reasoning layer

An answer you can defend to a board — or an auditor.

The AI across every surface is not a chatbot wrapper. It is a discipline: graph retrieval, a library of vetted queries, structured outputs, and mandatory citation — source rail, source table, row count — behind three trust tiers. Every claim carries its tier, in the open.

A1 · highest

Expert-verified

Reviewed by a credentialed expert and confirmed across more than one regulator. The bar for a claim that carries real weight.

A2

Cross-source matched

AI-reviewed and matched across more than one independent source, so the record agrees with itself before it stands.

A3

Single-source

AI-reviewed against one authoritative source — shown as exactly that, never dressed up as more than it is.

Access

An open reference floor. A commercial layer above.

Safety data is free on every profile — always. Researchers, students, and the public get the open, citable catalogue; the teams who buy and oversee get the deep intelligence. That open floor is how the reference earns the citations that make it the thing everyone reaches for in the same week.

Open · free
For researchers & the public
  • Core reference across the rails
  • Safety data free on every profile
  • Citable, with stable identifiers
Browse the rails →
Institutional
For teams who buy & oversee
  • Full search, exports, and alerts
  • The rail's deep intelligence
  • Cross-regulator coverage
Request access →
Enterprise
For systems that build on it
  • API access & custom integration
  • SLA and dedicated support
  • Data-residency options
Talk to us →

The rails are request-access while v1 finalizes; pricing scales with coverage, not seats. Oushvaa Procure publishes transparent pricing on its own surface — every rupee, justified.

By the numbers

Built, not promised.

Live-verified counts across the rails — every figure traceable to a regulator, statute, or safety database. India is the source-of-truth market; global is the reach. Never rounded up.

75.5M
FAERS drug-event records
Drawn from 20.3M underlying FDA reports — queryable for signal and co-occurrence.
5.09M
Device records
Across 6 registries — FDA, EU, CDSCO, Health Canada, PMDA & TGA — with 23.4M adverse-event records.
597,711
Canonical drug records
Salt-canonicalized; 6,768 built to full label-deep profiles.
66,252
Canonical companies
The entity graph that links one company across every rail.
20
Regulators
Approval data crosswalked, India-first, to FDA · EMA · WHO.
India-first
Structurally global
National registries linked to the global authorities, one record at a time.
Trust

Built audit-grade.

Least-privilege by default, published policies, and provenance on every figure. An open reference floor — catalogue and safety data are searchable; deep intelligence and the full corpus stay gated. Customer data is isolated by tenant: a hospital's records never leave its account and are never shared or sold; only de-identified, aggregated benchmarks flow back.

Policies
26 published
Security and data-handling policies, published in the trust center.
Data
Open floor + gated
Safety data free on every profile; customer data isolated by tenant.
Security contact
Published
A named contact and a responsible-disclosure path.
Tenant isolation & least-privilege by defaultin force
Pooled benchmarks, never individual recordsin force
Source-traced provenance on every figurein force
India data residencyin force
SOC 2 — Type Iroadmap