Products

Three operating systems.
One governed platform.

ClinicalOS runs your trials, DiligenceOS runs your deals, and Voice IQ runs your voice outreach. Each one automates work your team does by hand today, inside your own environment, with every answer traced to its source.

Your environment
Data stays inside

One governed platform. Three operating systems on top of it.

50%
Shorter proposal cycles
100%
Answers cited to source
95%
Lower cost per patient check-in
4–8 wks
From kickoff to live deployment
The product suite

Purpose-built for three hard jobs.

Not a general-purpose assistant. Each product is built around a specific workflow, with the compliance and evidence trail that workflow demands.

Clinical research

ClinicalOS™

Win more bids. Run faster trials.

The operating system for CROs and sponsors. It drafts regulatory-ready protocols, validates feasibility against live global registries, and keeps recruitment moving — so proposals go out in hours instead of weeks.

  • Regulatory-ready protocols drafted in hours
  • Feasibility checked against live global registries
  • Automated patient-to-site matching from EHR data
  • Connects to your existing CTMS and eTMF

CROs · Sponsors · Clinical research teams

50%shorter proposal cycles
Explore ClinicalOS
Due diligence

DiligenceOS

From data collection to deal execution.

The operating system for high-stakes due diligence. It turns a static data room into a living, queryable report that investors interrogate in plain English — with every answer traced to the exact page it came from.

  • Connects to SharePoint, dealrooms and internal servers
  • Living reports that update as new material lands
  • Investors get source-cited answers on demand
  • Tiered, per-investor access you control

Founders · VCs · Angel and investor networks

100%of answers cited to source
Explore DiligenceOS
Voice outreach

Voice IQ

Outreach calls that run themselves.

An automated voice outreach agent for high-volume, structured outbound calling, with the script, language set and compliance profile configured per deployment. It runs today in clinical patient follow-up and government citizen outreach.

  • Configured per deployment: script, language, exports
  • Citizen outreach in English and 8 Indian languages
  • Clinical patient follow-up runs in English today
  • Adverse event alerts, with PDF, CSV and SDTM-ready export

Clinical sites · Coordinators · Public-sector teams

92–98%follow-up compliance rate
Explore Voice IQ
Why teams pick Enclavia

Built for work that gets audited.

Clinical trials, investment decisions and patient safety all get reviewed after the fact. Every product is built so the review is straightforward.

Your data stays yours

Deployed inside your environment, with PHI redacted before anything leaves the record.

Built for regulators

HIPAA, SOC 2, GDPR and FDA 21 CFR Part 11, with a complete audit trail on every decision.

Every claim sourced

Answers cite the exact document and page, so any line can be verified by a reviewer.

Live in weeks, not quarters

Four to eight weeks from kickoff to a working deployment on your own data.

“What used to take 2 people × 10 days, we now complete in minutes with 1 person.”

— CEO, MedTech customer

Measured across deployments

95%
Data-room ingestion accuracy
3.5×
Clinical efficiency gain
57%
Faster study database locks
15–20%
Manual charting error rate removed

Languages set per deployment

Government and citizen outreach runs multilingual: English plus eight Indian languages — Hindi, Gujarati, Telugu, Marathi, Tamil, Kannada, Bengali and Punjabi. Clinical patient follow-up runs in English today.

Regulator-ready by default

HIPAA, SOC 2, GDPR, FDA 21 CFR Part 11 and FedRAMP-aligned, with signed records and cryptographically secured vaults.

Fits the systems you run

Native connections into existing CTMS and eTMF, SharePoint, virtual data rooms and proprietary internal servers.

Getting started

From briefing to live in weeks.

Start with one workload that already costs you money, prove the numbers against your own baseline, then scale.

Briefing · 30 minutes

We map the right product to one workload you own — an active RFP, a live data room, or a running study — and agree the numbers it has to beat.

Proof of concept · 4–8 weeks

Your data, your environment. We run it alongside your current process and measure cycle time, cost and accuracy against your existing baseline.

Rollout · and scale

Go live on the workload that proved out, then add engines and agents module by module — every one governed, audited and traceable.

Common questions

What buyers ask before a pilot

Still have questions?

Our team is ready to help — let’s get you set up.

Contact our team