Why nowPlatformWorkflow CoverageEnterprise Try the grader
AI Marketing Governance for Healthcare

Ship healthcare marketing
that's compliant, before it goes live.

AI-powered marketing compliance across jurisdictions. Check any asset — copy, design, whitepaper, video or live page — against the requirements that apply in your market: the United States (FDA, FTC, HIPAA) and India (ASCI, CCPA, CDSCO, NMC, FSSAI). Every finding cites its source.

SOC 2 Type II HIPAA-ready Every finding cites its source US & India jurisdictions No asset stored without consent

Built for compliance & marketing teams in regulated healthcare

Northwind PharmaHelix BiotechMeridian HealthCareBridge Vantage MedtechOakline HospitalsLumen TherapeuticsBlueRiver Agency Northwind PharmaHelix BiotechMeridian HealthCareBridge Vantage MedtechOakline HospitalsLumen TherapeuticsBlueRiver Agency
The cost of the status quo

Compliance review is where healthcare marketing goes to wait.

Every campaign queues behind a shared inbox, a spreadsheet, and three reviewers in different time zones. The delay is not the worst part — the missed risk is.

0

Median time from draft to approved in a regulated marketing team.

Manual review 19 days
With RegulaAI 38 seconds

Risk hides in volume

One campaign is 40+ assets across 6 channels and 5 markets. Human reviewers see a fraction and sample the rest.

Where reviews fail

Findings across 12,400 graded assets.

3.2kfindings
Efficacy claims · 46%
Disclosure gaps · 31%
Regional rules · 23%
0

Assets per campaign

0

Channels to police

0

Regulators in play

0

Typical enforcement exposure

The platform

One system that reviews, routes,
and proves compliance.

Not a checklist. A grounded, multi-jurisdiction rule engine that reads any asset, applies the framework for your selected market, cites the regulation behind every flag, and rewrites the copy to be compliant by construction. RegulaAI provides AI-assisted compliance analysis and does not constitute legal advice.

Grade any asset — not just text

Paste copy, upload a design, a PDF whitepaper, a case study, a Word doc or a video, or point it at a live URL. RegulaAI extracts the content and grades it against the full corpus.

Design Whitepaper Case study Video Live URL

Every flag cites its source

Each finding links to the exact regulation — 16 CFR §255.5, FTC Act §5 — not a vague warning. Auditable by design.

Compliant-by-construction rewrite

One click turns a flagged asset into publish-ready copy: claims softened, disclaimers added, score re-checked live.

Seconds, not sprints

0

Median full review, end to end.

Tamper-evident audit trail

Every grade, edit, and human approval is appended to a signed chain — the record that proves a qualified human signed off.

01 — INGEST

Drop in anything.

Ad copy, a Figma export, a 40-page whitepaper, a case study, a product video, or just a live URL. RegulaAI extracts the words wherever they live — OCR on designs, text layers from PDFs, transcripts from video.

DesignPDFDOCXVideoLive URL
02 — REVIEW

Six reviewers, in parallel.

Claims, privacy, disclosure, regional, brand and audit reviewers each grade the asset simultaneously against 56 cited rules. What took three reviewers three weeks resolves in under a minute.

FDAFTCHIPAAEMAMHRA
03 — EXPLAIN

Every flag cites its source.

Not "this looks risky." A prioritised list with the exact phrase that tripped, the regulation behind it — 16 CFR §255.5, FTC Act §5 — a link to the statute, and the precise fix.

TraceablePrioritisedAuditable
04 — RESOLVE

Publish-ready in one click.

Generate a compliant rewrite with claims softened and disclaimers added, re-score it live, route it to a human for sign-off, and append the decision to a tamper-evident chain.

RewriteRe-scoreSigned
Specialised reviewers

Six reviewers for every layer
of healthcare risk.

Generic copy checkers don't know what a "claim" means in healthcare. Each RegulaAI reviewer is tuned to one regulatory dimension and runs in parallel.

Claims Analyst

Detects efficacy, superiority and outcome claims that need competent and reliable substantiation.

FTC Act §5 · FDCA

Privacy Guardian

Flags PHI exposure, patient imagery and testimonial usage that breaches privacy rules.

HIPAA · GDPR

Disclosure Checker

Catches missing material connections, paid endorsements and required safety information.

16 CFR §255

Regional Specialist

Applies the right rulebook per market — what clears in the US may trip in the EU or UK.

EMA · MHRA · TGA

Brand & Tone

Enforces your internal policy alongside regulation, so legal and brand agree in one pass.

Custom rule sets

Audit Scribe

Writes the defensible record: what was flagged, what changed, who approved, and when.

Tamper-evident log
The workflow

From draft to approved,
without the back-and-forth.

RegulaAI advises; a qualified human decides; the audit trail proves it. That order never changes.

1

Drop in any asset

Paste copy, upload a design or whitepaper, or paste a live URL. Extraction happens automatically.

Instant
2

Six reviewers run in parallel

Claims, privacy, disclosure, regional, brand and audit reviewers grade simultaneously against 56 cited rules.

~38 seconds
3

Get a score and prioritised fixes

A 0–100 risk score with blocking issues first, each showing the matched phrase, the regulation, and the exact fix.

Every fix cited
4

Rewrite to compliant in one click

Generate publish-ready copy with claims softened and disclaimers added, then re-score it instantly.

Compliant by construction
5

Route for human approval

Send to the right reviewer with full context. Approve or send back — the decision is appended to the audit chain.

Signed & logged
Global coverage

Every market you sell in.
Every rulebook that governs it.

Select your market and RegulaAI applies that jurisdiction's framework — so a campaign that clears in the US doesn't quietly breach the ASCI Code or the Drugs and Magic Remedies Act in India. United States and India are live today.

USFDA · FTC · HIPAA56 rules live
INASCI · CCPA · CDSCO · NMC · FSSAI29 rules live
EUEMA · EFPIALive
UKMHRA · ASA CAPLive
AUTGALive
+35Additional marketsOn the roadmap
Governance analytics

Compliance you can measure,
not just trust.

Show the board risk trending down, first-pass approval trending up, and an audit chain that is provably intact.

First-pass approval rate

Since deploying RegulaAI across four brand teams.

FebMarAprMayJunJulAug
0

First-pass approved

0

Blocking issues caught

0

Faster than manual

0

Findings traceable to source

From the teams

Faster launches. Fewer surprises.

"

We cut our MLR cycle from three weeks to the same afternoon. The part legal cared about was that every flag cites the actual regulation.

PN
Priya NairHead of Compliance, Halcyon Health
"

The rewrite feature is the unlock. It doesn't just tell you the claim is wrong — it hands you copy you can actually publish.

ML
Marcus LeeVP Marketing, Northwind Dermatology
"

Running one asset against five markets at once used to be a spreadsheet and a prayer. Now it's a single click and a signed record.

AK
Aisha KhanGlobal Brand Lead, Meridian
Enterprise & security

Everything IT, security
and legal will ask for.

SSO & RBAC

SAML / OIDC single sign-on with role-based access down to the rule set.

SOC 2 Type II

Independently audited controls, penetration tested, continuously monitored.

Data residency

Choose where assets are processed and retained. Nothing stored without consent.

Fits your stack

Connect the CMS, DAM, and workflow tools your team already uses — plus a browser extension that reviews in context, wherever you write.

Your policies, encoded

Layer internal brand and legal standards on top of the regulatory corpus, so one review satisfies both.

Questions

Everything you're wondering, answered.

Does RegulaAI replace our legal and medical reviewers?
No. It removes the repetitive work so your experts focus on the genuinely hard calls, with full context and an audit trail. RegulaAI is assistive, not authoritative — a qualified human always decides.
How current are the rules?
The corpus is maintained continuously and versioned. When a regulator publishes new guidance, the rule is updated and republished to every tenant, with the change recorded in version history.
Which countries and regulators are covered?
40+ countries and 15+ regulators including FDA, FTC, HIPAA, EMA, MHRA, TGA and Health Canada, expanding on a rolling basis.
Where does our data go?
Assets are processed securely and never retained without consent. Data residency is configurable on enterprise plans, and the browser-based grader processes content locally.
How long does setup take?
Most teams grade their first asset within minutes of signing in. Integrations and SSO are configured during onboarding, typically within a week.
Can we encode our own internal policies?
Yes. Custom rule sets let you enforce brand and internal standards alongside regulatory ones, so a single review satisfies legal and brand at once.
See it on your own assets

Grade a real campaign
in the next two minutes.

Open the workspace, paste your copy or drop in a design, and watch it score against 56 cited rules — with the exact fixes, and a compliant rewrite.