iso-standards-readiness – skill Lập trình cho agent AI

ISO Standards Readiness Evidence Preparation

Purpose

Use this skill to organize declared scope, controlled documents, implementation

records, traceability, and readiness evidence for substantive human review against a

named standard. It summarizes process workflows and provides deterministic local

checks. It contains no clause text and performs no audit.

SKILL.md holds the boundary, lane discipline, shared evidence workflow, and CLI

contract. Per-standard preparation details live in references/.

Non-negotiable boundary

This skill cannot:

• certify or accredit anything, issue or validate a certificate, accreditation

schedule, or licence, or promise an audit, assessment, or inspection result;

• determine legal/regulatory applicability, device classification, reportability,

conformity route, product authorization, market access, licensure, personnel

qualification, or compliance;

• replace authorized management, the management representative, laboratory director,

quality manager, authorized signatory, RA/QA, legal counsel, regulatory/competent

authorities, a notified body, an MDSAP Auditing Organization, an accreditation body,

an assessor, or a certification body;

• validate a method, compute or approve measurement uncertainty, establish

metrological traceability, set risk-acceptability criteria, or judge whether a risk,

decision rule, or reference interval is fit for purpose; or

• infer implementation, competence, conformity, compliance, or readiness from a

template, checklist, filename, keyword, document count, percentage, or script

result.

Always label outputs **draft evidence-preparation material for authorized human

review**. Preserve unresolved decisions as blockers rather than resolving them.

ISO and IEC copyright

ISO and IEC standards are copyrighted. Obtain each standard from

[ISO](https://www.iso.org/standards.html), IEC, an ISO national member, or another

authorized source. Do not retrieve, paste, reproduce, or generate clause text.

Summarize the organization's own process and cite the controlled authorized copy. See

[ISO copyright](https://www.iso.org/copyright.html). Accreditation-body, CAP, and

scheme checklists that quote requirements are separately licensed — keep them out of

shared repositories and prompts too.

Standards covered

Read the reference file for the standard in play before preparing evidence. Each

one carries its own current edition, lane, domain vocabulary, and failure modes.

| Standard | Profile key | Lane | Reference |

| --- | --- | --- | --- |

| ISO 13485 medical device QMS | iso-13485 | Certification | references/iso-13485.md |

| ISO 14971 device risk management | iso-14971 | Supports a declared lane | references/iso-14971.md |

| ISO/IEC 17025 testing and calibration laboratories | iso-17025 | Accreditation | references/iso-17025.md |

| ISO 15189 medical laboratories | iso-15189 | Accreditation | references/iso-15189.md |

A standard absent from this table is out of scope for the bundled checks. Do not

repurpose a profile for a standard it does not name — a domain vocabulary borrowed from

a different standard produces a report that looks complete and means nothing.

Current baseline (read the ledger before any time-sensitive statement)

• ISO 13485:2016 Edition 3, confirmed after its 2025 systematic review.

EN ISO 13485:2016/A11:2021 is a European amendment, not an ISO international

"Amendment 1:2021."

• ISO 14971:2019 Edition 3, confirmed in 2025, with ISO/TR 24971:2020 as its

informative guidance companion. Its proposed successor ISO/AWI TS 24971-1

is under development, not a published replacement or a new normative basis.

• ISO/IEC 17025:2017 Edition 3 remains current; no successor edition identified.
• ISO 15189:2022 Edition 4 replaced the 2012 edition, absorbed the POCT

requirements formerly in ISO 22870, and its accreditation transition closed in

December 2025 — implemented, not upcoming.

• FDA QMSR effective and enforced since 2026-02-02; Part 820 is titled

*Quality Management System Regulation*; QSIT is retired in favour of Compliance

Program 7382.850.

• MDSAP current Audit Approach is MDSAP AU P0002.011, version date

2026-08-03.

• Accreditation recognition: Global Accreditation Cooperation Incorporated

commenced full operations 2026-01-01, replacing ILAC and IAF, with its own MRA;

former IAF MLA / ILAC MRA outputs stay recognized during the transition.

• EU: use current consolidated MDR/IVDR texts, current OJEU harmonised-standard

decisions, current MDCG guidance, and the product-specific conformity route.

Read references/source-ledger.md before making any time-sensitive statement. It

records catalogue confirmation, published versus draft documents, and the remaining

EU source-retrieval limitations. The bundled report basis_date is this skill

release's research baseline, not the organization's review date or a freshness guarantee.

Keep the assurance lanes separate

Lane confusion, not missing documents, causes most substantive errors here.

Certification, accreditation, regulator inspection, mandatory licensure, regulatory

audit programmes, and product conformity assessment are decided by different bodies

against different bases, and none substitutes for another. Two rules that are violated

constantly:

• Organizations are certified; laboratories are accredited. "ISO 17025

certified" and "ISO 15189 certified" are category errors.

• A certificate never displaces a regulator. ISO 13485 certification does not exempt

anyone from FDA inspection, and ISO 15189 accreditation does not satisfy CLIA.

Read references/assurance-lanes.md for the full lane table, scope-statement limits,

and the titling rule.

Core workflow

Step 1: Declare the standard, purpose, and authorized owners

Name the standard(s), the lane(s) the work supports, and the owners: management

representative or laboratory director, quality owner, legal/applicability owner,

process or technical owners, approvers, and escalation route. A lane is a declared

input, never an inference.

PYTHONDONTWRITEBYTECODE=1 python3 scripts/validate_scope_intake.py \
  assets/templates/scope-intake-template.json --standard iso-13485

Use the matching template and profile:

| Profile | Template |

| --- | --- |

| iso-13485, iso-14971 | assets/templates/scope-intake-template.json |

| iso-17025 | assets/templates/laboratory-scope-intake-template.json |

| iso-15189 | assets/templates/medical-laboratory-scope-intake-template.json |

--standard defaults to iso-13485. Every distributed template intentionally fails

closed; copy it outside the skill and complete it with controlled organizational

evidence. Undetermined applicability raises HUMAN_DECISION_REQUIRED — leave it as a

blocker.

Step 2: Freeze source/version evidence

For every standard, regulation, guidance, scheme document, audit model, and product

source, record publisher, official title, edition/version/date, authorized location,

access and currency-review dates, scope/applicability owner, impact assessment, status,

evidence, and approval.

Do not use search snippets as controlled requirements. Do not silently update an

incorporated edition when a publisher releases a new one — FDA incorporated a specific

ISO 13485 edition, and a later ISO or EN publication does not change it.

Step 3: Inventory controlled documents and records

Do not count named procedures or scan keywords. Build an explicit register linking

documents, records, source versions, owners, approvals, effective dates, retention

bases, training, and change records.

PYTHONDONTWRITEBYTECODE=1 python3 scripts/audit_document_records.py \
  assets/templates/document-register-template.json

This check is standard-agnostic. Read references/evidence-architecture.md for the

evidence architecture.

Step 4: Review process implementation

Assess controlled procedures and sampled records across the domains your profile

declares — the per-standard reference file lists them. Each item needs owner, status,

evidence IDs, source/version, approval, and open-gap links.

A procedure describing an activity is not evidence the activity happened. Sample

records in every domain you report on, and state what you sampled and what you did not.

Step 5: Run the focused checks that apply to the lane

Device lanes (iso-13485, iso-14971) — risk/design/production/post-market chain:

PYTHONDONTWRITEBYTECODE=1 python3 scripts/check_traceability.py \
  assets/templates/traceability-matrix-template.json

All standards — corrective action and effectiveness:

PYTHONDONTWRITEBYTECODE=1 python3 scripts/check_capa.py \
  assets/templates/capa-record-template.json

All standards — suppliers and externally provided products and services, including

calibration providers, reference-material supplie

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