# Compliance > Use when scoping which regulatory frameworks bind a business — SOC 2, ISO 27001, HIPAA, PCI DSS, EU AI Act, DORA, NIS2 — building a control register with owners and evidence, or standing up the cadence that keeps it audit-ready. NOT drafting privacy-policy/ROPA/DPA or ToS text (that is gdpr-privacy, terms-conditions), NOT hardening code (that is secure-coding). - Skill: `ericrisco/compliance` (Agent Skill, multi-file: 6 files) - Install (CLI): `npx skillmds@latest add ericrisco/compliance` - Raw SKILL.md: https://api.skillmd.com/api/skills/ericrisco/compliance/raw - Safety review: pending - Works with: Claude Code, Claude.ai, OpenAI Codex - Category: Security - Author: ericrisco (https://skillmd.com/u/ericrisco) - Updated: 2026-09-17 - Page: https://skillmd.com/skills/ericrisco/compliance --- # Compliance — scope the frameworks, build the register, run the rhythm You turn a vague "we need to be compliant" into artifacts that survive an audit: a scoped framework list with current deadlines, a **control register** (one row per control, tagged to every framework it satisfies, each with an owner and an evidence source), a **cadence calendar** of the recurring work that keeps the program true between audits instead of scrambling once a year, and an evidence-source catalog. Your job is **scoping and orchestration, not legal opinion**. You map the business to the frameworks, build the register, assign owners and cadences, and stand up the rhythm. You do not give legal advice; flag where a licensed specialist or auditor must sign off. **Route out** — these are owned by siblings, not by you. You *reference* the resulting documents as evidence sources in the register; you do not write them here. - Privacy notice, ROPA, DSAR flow, consent banner → `../gdpr-privacy/SKILL.md`. - Terms of Service, EULA, acceptable-use → `../terms-conditions/SKILL.md`. - Internal retention/classification policy *text* → `../data-policy/SKILL.md`. - Commercial contract / MSA / DPA clause drafting → `../contracts/SKILL.md`. - Hardening the code (authn, secrets, injection, headers) → `../secure-coding/SKILL.md`. ## Step 1 — Scope to the frameworks that actually bind Do not copy a framework because a competitor has it. Map business attributes to obligations. Ask the operator the attribute questions, then apply this table. | Business attribute | Framework that binds | Current deadline / status (as of 2026-06-02) | | --- | --- | --- | | Sells SaaS to enterprise / asked for a security report | SOC 2 (Security TSC mandatory) | Type II window 3–12 months; pick scope before you start | | Wants an internationally recognized ISMS certificate | ISO/IEC 27001:2022 | 93 Annex A controls, 4 themes; 2013→2022 transition deadline **passed 31 Oct 2025**, all live certs are 2022 | | Stores / processes / transmits cardholder data | PCI DSS v4.0.1 | **Fully mandatory since 31 Mar 2025** — ~50 former "best practice" items (MFA on all CDE accounts, automated log review, internal vuln scans, periodic account reviews, asset inventory) are now hard requirements | | Touches US protected health information (PHI/ePHI) | HIPAA Security Rule | In force today. A **2024 NPRM is NOT yet finalized** (mid-2026) — flag forthcoming, but note OCR is already citing the proposed standard in enforcement | | Handles personal data of EU/EEA users | GDPR (as a control source) | In force; feeds controls (access, breach notice, vendor DPAs). Document *text* → `../gdpr-privacy/SKILL.md` | | Builds or deploys an AI system, esp. high-risk use | EU AI Act | Phased — see below; **2 Aug 2026 is the active legal date** for Annex III high-risk | | Is an EU financial entity (or critical ICT vendor to one) | DORA | **In force since Jan 2025** — ICT risk mgmt, incident reporting, resilience testing, third-party risk | | Operates essential/important services in the EU | NIS2 | Transposed in 21/27 member states by Mar 2026; many set a first audit deadline of **30 Jun 2026** | **EU AI Act — get the dates exactly right (high audit risk):** - Prohibited practices + AI-literacy: **2 Feb 2025**. - GPAI-model obligations + governance + penalties: **2 Aug 2025**. - Annex III (use-based) high-risk obligations: **2 Aug 2026**. - Annex I (product-regulated, incl. medical devices): **2 Aug 2027**. - The **Digital Omnibus on AI** (provisional trilogue agreement **7 May 2026**) proposes deferring Annex III to **2 Dec 2027** and Annex I to **2 Aug 2028** — but this is **NOT yet adopted**. Until the amendment is published in the Official Journal, **2 Aug 2026 remains binding.** Plan to the original date; flag the deferral as forthcoming-not-final. - Fines: up to **EUR 35M or 7%** of global turnover (prohibited use), up to **EUR 15M or 3%** (high-risk non-compliance). **Rule: treat a not-yet-adopted amendment or an NPRM as forthcoming, never as law.** Why: scoping to a draft that slips leaves you out of compliance on the date that is actually still in force. See `references/frameworks.md` for the per-framework control summaries. ## Step 2 — Build the control register One row per control. The register is the source of truth; everything else (checklists, audit responses, the cadence calendar) is generated from it. | Column | What goes in it | | --- | --- | | `control-id` | Stable internal id, e.g. `AC-02` | | `framework` | Every framework this control satisfies (multi-tag) | | `owner` | A named person/role accountable — never "the team" | | `evidence` | The exact artifact that proves it, and where it lives | | `cadence` | How often it is reviewed, sized by risk | | `last-verified` | Timestamp of the last attestation | | `status` | `met` / `gap` / `in-progress` | **Bad → Good control:** ```text Bad: "We do access control." (no owner, no proof, not testable) Good: AC-02 | ISO A.5.18 + SOC2 CC6.2 + PCI 7.2 | owner: Head of IT | evidence: quarterly IdP access-export reviewed & signed | cadence: quarterly | last-verified: 2026-05-30 | status: met ``` The Good row is auditable: an auditor can ask the owner for the dated export and verify the claim in minutes. **Exploit the overlap — one control, many frameworks.** SOC 2 and ISO 27001 overlap **~60–70%** (risk assessment, access management, incident response, logging, change management, vendor management all count toward both). So: - **Bad:** maintain a separate register per framework → the same control gets re-documented 3 times and drifts out of sync. - **Good:** one register, each control tagged to *all* frameworks it satisfies. Generate the per-framework checklist as a filtered view. ## Step 3 — Stand up the operating rhythm Audit-readiness is a continuous state, not an annual project. Emit a cadence calendar and put the recurring work on real dates with owners. | Cadence | Recurring compliance work | | --- | --- | | Daily | Automated control monitoring / alerting (failed logins, drift) | | Weekly | **Control-health review** — the heartbeat: walk open gaps, stale evidence, overdue owners | | Monthly | Evidence refresh for high-risk controls; vulnerability-scan review | | Quarterly | Access recertification; vendor/third-party risk reassessment | | Annual | Full risk assessment; policy review; penetration test; audit prep | The **weekly control-health review** is the single habit that kills the annual scramble. Why: a gap caught weekly is a five-minute fix; a gap discovered during the audit window is a finding. The full calendar, register schema, and audit-prep runbook live in `references/operating-rhythm.md`. ## Step 4 — Evidence discipline Evidence is what an auditor tests. Every piece must be: - **Timestamped** — undated evidence proves nothing about *when* the control ran. - **Mapped to the requirement** — link the artifact back to the framework clause (e.g. this export proves `ISO A.5.18` *and* `SOC2 CC6.2`). - **Owner-attested** — the named owner signs/confirms it, so accountability is traceable. - **Refreshed on cadence** — point-in-time evidence rots; a screenshot from last year does not prove a control operated *over* the audit window (Type II tests operating effectiveness across 3–12 months, not a single moment). Store evidence where it is findable on demand, not assembled in a panic the week before the auditor arrives. ## Anti-patterns | Anti-pattern | Why it fails | Do instead | | --- | --- | --- | | Checklist with no owners | "Everyone's job" means no one's job; the auditor asks who, and the room goes silent | Every control names one accountable owner | | Copying a framework you don't fall under | Wastes months certifying SOC 2 when the binding obligation was PCI DSS | Scope from business attributes (Step 1) first | | Treating an NPRM / not-yet-adopted amendment as law | The draft slips; you're non-compliant on the date still legally in force | Plan to the active date; flag drafts as forthcoming | | Point-in-time evidence | A single screenshot can't prove a control operated over the Type II window | Timestamped, periodic, owner-attested evidence | | One register per framework | Same control re-documented 3× and drifts; the 60–70% overlap is wasted | One register, each control multi-tagged | | Annual evidence scramble | Gaps surface as audit findings instead of weekly fixes | Weekly control-health review + cadence calendar | | Drafting the privacy policy / DPA here | That's legal-document substance, a different skill's lane | Route to `../gdpr-privacy/SKILL.md` / `../contracts/SKILL.md` | | Giving a legal opinion | You scope and orchestrate; you are not counsel | Flag where a licensed specialist or auditor must sign off | ## Verify `scripts/verify.sh ` lints a control register (Markdown table or CSV): it checks the required columns exist and that no row is missing an owner, evidence, or cadence — the cardinal sin of checklist theater. Read-only, exits 0 on a clean or empty register.