—— FOR CLINICAL TEAMS

Your clinical trials. Faster execution. Fewer documentation delays.

CARA manages your full Clinical function on one governed platform, CTMS, eTMF, eTMF Archive, and Medical Writing. Add CARA AI when you’re ready. CSR and synopsis writing effort reduced by 50–70%, patient narratives auto-drafted, and protocol consistency checked automatically.

Data never leaves CARA

Full audit trail on every AI output

One validation scope — total

Permissions apply automatically

—— THE PROBLEM

Your clinical team's expertise is going on documentation. Not on running the trial.

Protocol amendments, label updates, deviation reports — each one creates a reconciliation cascade across documents that don’t update themselves. Expert clinical time goes on checking alignment, not running the trial.

Clinical Ops Lead · Medical Writer · eTMF Manager

Most AI tools sit on top of that same fragmented foundation. Your team still has to chase the source, reconcile versions, and govern outputs separately. You’ve added a tool. You haven’t removed the problem.

CARA AI works from inside your clinical data not on top of it. The reconciliation work disappears. Your team gets back to the trial.

Built on unified Regulatory data

Trust, control, confidence by design

Productivity that was impossible before

OUTCOMES

The numbers that matter to Clinical.

50-70%

CSR and synopsis writing effort reduction

Auto

Patient narratives drafted from structured data

0 Manual data exports, one governed clinical layer

Continuous

Inspection readiness, no manual audit prep

GENERATE

Patient narratives drafted before your team starts writing

Auto-drafting patient narratives used to mean days of identical formatting work. CARA AI drafts them directly from structured clinical data; consistently formatted, traceable to source, ready for review not creation.

Manual drafting → Auto generated

COMPARE

Protocol consistency checked across every document. Automatically

Three versions of the protocol, a CSR, and an Investigator Brochure; keeping them aligned used to mean manual cross-referencing. CARA AI identifies semantic changes and misalignment simultaneously, before they reach regulators.

Days→ Automatic

PREDICT

Deviation patterns surfaced before they become inspection risk

Individual deviations look random. Patterns across a trial don't. CARA AI analyses deviation data continuously to surface systemic risks early; so your team intervenes before the pattern becomes a finding.

Reactive review → Early intervention

Clinical capabilities

What your teams sees

One governed AI layer across Regulatory, Safety, Quality, and Clinical, full traceability on every output.

Context aware search

Finds regulatory precedents and clinical correlations keyword search misses. Better decisions, complete information.

Automated classification

Every document tagged, categorised, and enriched automatically. Instant retrieval, every time.

Data extraction

Pulls structured data from messy PDFs and clinical reports. Analysis-ready outputs in seconds.

Pre-tuned for compliance

Built-in prompts for regulatory workflows. Accurate results from day one, or customise further

Your LLM

Choose the model that fits your needs. All processing stays in our secure framework. Your IP stays yours.

Source citations visible

Every output references the exact platform record it drew from.

Audit trail in the sidebar

Every output references the exact platform record it drew from.

Human review step built in

Every output references the exact platform record it drew from.

What becomes possible when all
your data is on one platform.

CARA AI runs on one platform. One validation scope.The AI capabilities extend what the platform already does,
no separate system, no separate contract, no separate validation cycle.

The more of your operations run on CARA, the more your AI can do. Regulatory, Safety, Quality, and Clinical on one platform
means AI that works across your entire function not just in silos.

Regulatory

For Regulatory Affairs & Reg Ops

Draft. HA query responses in 20 minutes

Generate. Submission dossiers from live data

Compare. Labels across all markets in 1 minute

Regulatory use case →

Safety

For Pharmacovigilance & PV teams

Generate. PSMF from live data, 3 weeks to minutes

Draft. PBRER and DSUR across your safety layer

Monitor. Signal detection across your full PV data

Safety use case →

Quality

For QA Managers & Quality Operations

Draft. SOPs and quality docs 50-80% faster

Detect. Change control, regulatory variation trigger

Audit. Full trail on every AI-generated output

Quality use case →

Clinical

For Clinical Operations & eTMF leads

Structure. eTMF AI classification and completeness

Inform. Regulatory submissions from eTMF data

Review. Trial master file gaps surfaced automatically

Clinical use case →

60%
of top pharma

1M+
Users

99.9%
Uptime SLA

Built on a platform that enterprise pharma already trusts

CARA AI runs on the same unified foundation already deployed across the world’s leading pharmaceutical companies. The platform that makes this AI possible has been proven in production, at scale, under inspection, across every major life sciences function.

25 +

Years in regulated life sciences

24/7

Expert Support

— PLATFORM ARCHITECTURE

One platform. One validation scope. No governance gaps.

Bolt‑on AI generates content in isolation. CARA AI generates it from your live, governed regulatory content with a complete audit trail, all within your current governance framework, without extra tools, exports, or revalidation.

HA Q&A answered in minutes — not days

A Health Authority query draws on live submission records, Safety data, and Quality records in a single response. No cross-system data pull. No manual reconciliation. One platform, one governed layer.
Metric: 2–5 days → 20 minutes
Label beneath metric: Based on internal benchmarks

Your clinical trials. Faster execution. Fewer documentation delays.

Your clinical team's expertise is going on documentation. Not on running the trial.

Built on unified Regulatory data

Trust, control, confidence by design

Productivity that was impossible before

OUTCOMES

The numbers that matter to Clinical.

50-70%

CSR and synopsis writing effort reduction

Auto

Patient narratives drafted from structured data

0

Manual data exports, one governed clinical layer

Continuous

Inspection readiness, no manual audit prep

GENERATE

Patient narratives drafted before your team starts writing

Auto-drafting patient narratives used to mean days of identical formatting work. CARA AI drafts them directly from structured clinical data; consistently formatted, traceable to source, ready for review not creation.

COMPARE

Protocol consistency checked across every document. Automatically

Three versions of the protocol, a CSR, and an Investigator Brochure; keeping them aligned used to mean manual cross-referencing. CARA AI identifies semantic changes and misalignment simultaneously, before they reach regulators.

PREDICT

Deviation patterns surfaced before they become inspection risk

Individual deviations look random. Patterns across a trial don't. CARA AI analyses deviation data continuously to surface systemic risks early; so your team intervenes before the pattern becomes a finding.

Clinical capabilities

What your teams sees

Context aware search

Automated classification

Data extraction

Pre-tuned for compliance

Your LLM

What becomes possible when all
your data is on one platform.

One platform. One validation scope. No governance gaps.

What Makes Us Different?

Purpose-Built AI for Life Sciences

Your clinical trials. Faster execution. Fewer documentation delays.

Your clinical team's expertise is going on documentation. Not on running the trial.

Built on unified Regulatory data

Trust, control, confidence by design

Productivity that was impossible before

OUTCOMES

The numbers that matter to Clinical.

50-70%

CSR and synopsis writing effort reduction

Auto

Patient narratives drafted from structured data

0

Manual data exports, one governed clinical layer

Continuous

Inspection readiness, no manual audit prep

GENERATE

Patient narratives drafted before your team starts writing

Auto-drafting patient narratives used to mean days of identical formatting work. CARA AI drafts them directly from structured clinical data; consistently formatted, traceable to source, ready for review not creation.

COMPARE

Protocol consistency checked across every document. Automatically

Three versions of the protocol, a CSR, and an Investigator Brochure; keeping them aligned used to mean manual cross-referencing. CARA AI identifies semantic changes and misalignment simultaneously, before they reach regulators.

PREDICT

Deviation patterns surfaced before they become inspection risk

Individual deviations look random. Patterns across a trial don't. CARA AI analyses deviation data continuously to surface systemic risks early; so your team intervenes before the pattern becomes a finding.

Clinical capabilities

What your teams sees

Context aware search

Automated classification

Data extraction

Pre-tuned for compliance

Your LLM

What becomes possible when all your data is on one platform.

One platform. One validation scope. No governance gaps.

What Makes Us Different?

Purpose-Built AI for Life Sciences

What becomes possible when all
your data is on one platform.