EU AI ACT / ARTICLE 50(4) / TAKES EFFECT 2 AUGUST 2026

Human content review and Article 50(4) compliance evidence for AI-generated text.

We do the actual review. We produce the documented evidence. You get an audit-ready compliance file you can hand to any regulator, enterprise customer, or auditor. Founded by a doctor, run by a network of credentialed reviewers.

Founding customer cohort opening Q2 2026. Procedure document and reviewer roster available on request. We are not a law firm.

THE GAP

The EU AI Act applies to your content. You probably do not have a compliance answer.

01 / EXTRATERRITORIAL REACH

It applies even if you are not in Europe.

Article 50(4) attaches to AI-generated text published to inform the public on matters of public interest. If your content reaches EU users, you are in scope. There is no carve-out for non-EU publishers, and the regulation tracks the audience, not the office address.

02 / THE DEADLINE

The transparency obligation takes effect 2 August 2026.

From that date, AI-generated text in scope must either be labelled as artificially generated, or fall under the human review exemption. Article 99 penalties run up to EUR 15M or 3 percent of global annual turnover. Reputational exposure exceeds the fine.

03 / NO OPERATIONAL TOOLING

System-level GRC vendors do not cover content.

Vanta and Drata cover SOC 2. Delve and Holistic AI cover the AI system. Nobody covers the article. There is no off-the-shelf product for "human reviewed this piece, here is the reviewer, here is the procedure, here is the evidence." That is the gap we close.

WHAT YOU GET

An audit-ready compliance file. Reviewed by named humans.

A continuing subscription that delivers the six documentation components an Article 50(4) human review claim is built on. Issued under your editorial designation, available on request to any regulator, customer, or auditor.

01 / PROCEDURE

Editorial Review Procedure

A 12-section written procedure document, customized to your publishing workflow, versioned and dated. The artefact a regulator asks for first.

02 / ROSTER

Named reviewer roster

The natural persons authorized to review your content, with credentials, languages, and signed reviewer agreements on file.

03 / DESIGNATION

Editorial responsibility designation

A written designation of the editorially responsible person for content under this engagement. Three configurations available: customer-side, Sygil-side, or shared.

04 / ATTESTATION LOG

Per-article attestation log

One signed attestation entry per article, with reviewer, timestamp, methodology version, and a hash that lets a third party verify integrity.

05 / EVIDENCE REPORT

Monthly evidence report

A bundled monthly report tying together the procedure version in force, the roster in force, and the attestation entries from that period.

06 / VAULT

Customer compliance vault

A secured store of every artefact above, queryable by article ID, exportable as a PDF package, retained for the regulatory limitation period.

SAMPLE ATTESTATION ENTRY
ATTESTATION_LOG / v1.0
ARTICLE_ID          : ART-2026-00471
CUSTOMER            : [REDACTED PUBLISHER]
REVIEWER            : K. Iyer, MBBS, Senior Medical Editor
REVIEW_TIMESTAMP    : 2026-04-07T11:42:18Z
METHODOLOGY_VERSION : ERP-2026-Q2.1
EDITORIAL_RESP      : Customer-side, designation on file
ATTESTATION_HASH    : 8a4f1c77e93b6d0e2a5c8f1b9d4e7a02
THE WORKFLOW

Five steps from intake to attestation.

A continuing service, not a one-time audit. Every article in scope flows through the same five steps before it publishes.

STEP 01

Scoping call

A 15-minute conversation to confirm you are in scope, identify which content surfaces are covered, and pick the editorial responsibility configuration that fits your structure.

STEP 02

Procedure customization

We adapt the standard 12-section Editorial Review Procedure to your publishing workflow, sign-off chain, and tooling. You get a versioned PDF and a markdown source.

STEP 03

Article intake

You submit articles via the intake endpoint (web, email, or API) before publication. Each piece is logged with a unique ID, source, intended publication date, and audience.

STEP 04

Human review

A named reviewer from your assigned roster reads the article against the procedure, applies the agreed methodology, and records the review decision with their credentials on the entry.

STEP 05

Attestation and delivery

A signed attestation is generated, hashed, written to your compliance vault, and returned to you. The article is cleared to publish under the Article 50(4) human review exemption.

See the full seven-step workflow ->

WHY Sygil

Why publishers choose Sygil.

Three things that no general compliance vendor, no AI detection tool, and no editorial agency can credibly offer in the same package.

REAL REVIEWERS

Named, credentialed, on the record.

Every reviewer on your roster is a named natural person with verifiable credentials, a signed reviewer agreement, and a photo on the team page. Not a model. Not an offshore mystery box. Real names a regulator can phone.

SPECIFIC REGULATION

We do Article 50(4). That is the entire product.

We do not sell general AI governance, model risk audits, or system-level posture management. One regulation, one obligation, one deliverable. The narrowness is the moat.

FOUNDER IS A DOCTOR

Editorial responsibility you can actually assign.

Editorial responsibility under the Code of Practice can sit with a credentialed individual. Our founder is an MD. The PhD network is real. Regulated verticals reward this in a way no SaaS competitor can copy.

THE WHY-NOW

Your enterprise customers are about to start asking.

EU enterprise procurement teams are already adding AI content questions to vendor questionnaires. Banks, pharma, media holding groups, and government tenders cite the AI Act in their 2026 vendor reviews. By Q3 2026 these questions are standard. A vendor who cannot answer them loses the deal, slows the renewal, and triggers a legal escalation every time. A vendor who can answer in one page closes faster. That one page is what we produce.

SAMPLE VENDOR QUESTIONNAIRE RESPONSE
Q14. DESCRIBE YOUR HUMAN REVIEW PROCESS FOR AI-GENERATED CONTENT.

A.   All AI-assisted text published on our properties is reviewed
     by a credentialed human reviewer prior to publication. Review
     methodology is documented in our Editorial Review Procedure
     v1.0 (Sygil, 2026). Per-article attestations are
     maintained in our compliance vault and are available on request
     under NDA. Editorially responsible person on file.

See sample vendor questionnaire responses ->

PRICING

Pick a plan that matches your publishing volume.

Annual subscriptions, article-capped tiers, transparent pricing. No fake discounts, no countdown timers. Full feature matrix and Enterprise tier on the pricing page.

STARTER
$5,000
per year, billed annually
Up to 60 articles per year. For solo operators, niche newsletters, and small content teams who need a defensible compliance file without enterprise overhead.
  • Up to 60 articles per year, Tier 1 review
  • Per-article attestation PDFs
  • Standard procedure document
  • Monthly compliance reports
  • Annual audit-ready bundle
  • 5 business day turnaround
Choose Starter
PREMIUM
$24,000
per year, billed annually
Up to 400 articles per year. For publishers at scale, healthcare and finance operators, and teams preparing for enterprise procurement gates.
  • Up to 400 articles per year
  • Tier 2 editorial review on all articles
  • Tier 3 subject-matter review on up to 50 articles
  • Custom procedure document
  • Multi-framework attestation (NIST AI RMF or ISO 42001)
  • 2 business day turnaround
  • Dedicated lead reviewer
Choose Premium

Publishing more than 400 articles a year? See the full feature matrix and Enterprise tier ->

Get a compliance answer before 2 August 2026.

Fifteen minutes on the phone. We confirm whether you are in scope, which tier matches your volume, and what the first 30 days look like. No commitment.

Book a 15-minute scoping call

15 minutes. No commitment. We will tell you if you are out of scope.