AI Act & NIS2 compliance readiness

Enterprise buyers ask structured questions before they sign. We build the evidence to answer them.

In 7–10 days, Model Evidence Advisory produces a practical AI compliance evidence room — structured documentation your team can use to respond to procurement, security, and regulatory readiness reviews.

Who this is for

European AI vendors at the point where enterprise buyers and regulated industries are asking structured questions about AI governance, security, and compliance readiness.

Organisations we work with

  • European AI vendors with B2B or enterprise sales
  • Product and operations teams receiving AI Act or NIS2-adjacent questionnaires
  • Founders and compliance leads without a dedicated legal or GRC function
  • Vendors preparing for regulated-sector procurement: financial services, health, public sector

What you are facing

  • Structured vendor questionnaires requiring AI governance responses
  • Requests for evidence of human oversight, risk management, or data practices
  • Compliance timelines that do not accommodate a multi-month project
  • No established internal process for generating reusable compliance documentation

The AI Compliance Evidence Room Sprint

A bounded engagement that produces a structured set of documentation your team can use and maintain across sales and procurement processes.

Inventory and mapping

  • AI systems inventory
  • AI Act preliminary classification mapping
  • NIS2 supplier readiness checklist
  • Risk and gap register

Documentation and response assets

  • AI use and human oversight policy drafts
  • Questionnaire response base (reusable)
  • Supplier evidence checklist
  • 30-day remediation roadmap

The evidence room is operational documentation — not a legal opinion, certification submission, or audit report. It organises what you have, identifies what is missing, and produces assets your team can use in sales and procurement processes.

How it works

The engagement begins with a paid diagnostic. The sprint is proposed only after the diagnostic is complete and reviewed. There is no obligation to continue beyond the diagnostic.

Paid diagnostic

You complete a structured intake questionnaire and submit relevant existing documentation. We review and produce a written diagnostic report identifying your current readiness position, key gaps, and applicable regulatory scope. The diagnostic is asynchronous; an optional 30-minute call is available. Diagnostic work begins only after payment is confirmed.

Sprint proposal

Based on the diagnostic findings, we produce a scoped sprint proposal covering deliverables, timeline, and pricing. You decide whether to proceed. No further obligation follows from the diagnostic.

AI Compliance Evidence Room Sprint

A focused 7–10 day engagement producing the documentation set described above. Delivered asynchronously with a structured handover. Your team owns and maintains the resulting documentation after delivery.

Diagnostic and sprint pricing

The diagnostic is the entry point to the engagement. Sprint scope is proposed after the diagnostic, using the official three-tier pricing structure below. Any beta discount is applied explicitly against these prices.

Paid diagnostic — beta entry point

€300 – €500

Exact fee is confirmed at booking. The diagnostic includes document review, a written readiness report, and a scoped sprint proposal. No sprint starts until scope and price are accepted. Beta pricing applies to bookings confirmed on or before 15 August 2026.

Official sprint tiers

  • Essential Evidence Pack: €1,500 — narrow buyer response and priority evidence gaps.
  • Standard Evidence Room Sprint: €3,500 — recommended for fragmented evidence and active enterprise procurement reviews.
  • Enterprise-Ready Evidence Room: €6,500 — repeatable readiness pack for multiple regulated enterprise buyers.
Request the diagnostic

Founder

Miguel Condeço

Model Evidence Advisory is founded by Miguel Condeço. The firm focuses on practical compliance readiness for AI vendors selling into enterprise and regulated markets. The firm works directly with founders, product, and operations teams to produce structured documentation that functions in real sales and procurement processes.

Contact

To request a diagnostic or ask a preliminary question:

miguel@modelevidenceadvisory.com

Response within 2 business days.

Disclaimer: Model Evidence Advisory provides readiness documentation, operational preparation, and structured evidence organisation. Services do not constitute legal advice, legal opinion, regulatory certification, compliance audit, or any guarantee of regulatory compliance. Clients should seek qualified legal counsel for legal and regulatory questions specific to their circumstances.