Start a free trial
Menu

STANAG 3318

STANAG 3318 Aeromedical aspects of aircraft accident and incident investigation

National militaries and organisations supporting aircraft accident and incident investigation under a contract or tasking that invokes AAMedP-1.7

STANAG 3318 is NATO's ratification agreement committing member nations to implement AAMedP-1.7, the Allied medical publication on aeromedical aspects of aircraft accident and incident investigation.

Edition
8
Published
2018-11-26
THIS DOCUMENT Agreement Holds requirements Organisation certificate Product or design assessed STANDARDIZATION AGREEMENT · EDITION 8 · 2018-11-26 STANAG 3318 Aeromedical aspects of aircraft accident and incident investigation STANAG 3318 is NATO's ratification agreement committing member nations to implement AAMedP-1.7, the Allied medical publication on aeromedical aspects of aircraft accident and incid. AGREEMENT STANAG 3318 The NATO agreement. The specification is not in this cover. WHERE THE REQUIREMENTS LIVE AAMedP-1.7 AAMedP-1.7 sets NATO's common format for the aeromedical information a national Aircraft Accident and Incident Investigation Board records after an aviation accident or in-flight a. The requirements live in AAMedP-1.7, not in STANAG 3318. Addressed to national authority. Puts AAMedP-1.7 into force. The document describes nations examining their ratification and reporting implementation details to the NSO, recorded in the NSDD; it names no certification or . Binds a nation once ratified. Reaches a supplier when a contract or national instruction names it or the publication it covers. Nobody is certified against this document. Nations report ratification; they do not issue a company certificate.

What it is

STANAG 3318 is the NATO Standardization Agreement by which participating nations commit to implement AAMedP-1.7, Edition B, the Allied medical publication covering aeromedical aspects of aircraft accident and incident investigation. This is Edition 8, promulgated 26 November 2018, and the document states plainly that it "supersedes the following document: STANAG 3318, Edition/Édition 7."

A STANAG is not the investigation manual itself

A STANAG is the agreement by which NATO nations commit to implement a standard, not the technical content itself. STANAG 3318's own text is short and administrative: an aim, an interoperability requirement, and the ratification, implementation and review machinery. "Participating nations agree to implement the following standard": AAMedP-1.7, Edition B. The publication's own content, the points to be covered in an aeromedical investigation, lives in that document, not in this cover agreement.

What it commits nations to

The stated aim is "to respond to the following interoperability requirements", and the requirement itself is "to standardize the essential points to be covered in the aeromedical investigation of accidents and/or incidents in order to facilitate the exchange of comparable information between nations and enhance interoperability." The cover also lists other related documents alongside AAMedP-1.7: STANAG 3531 (covered by AFSP-1.3), on safety investigation and reporting of accidents and incidents involving military aircraft, missiles and UASs; STANAG 7106 (covered by AAGSP-02), on the characteristics of breathing oxygen and its supply couplings; and ICAO Annex 13, on civil aircraft accident and incident investigation.

Who it binds, and how

STANAG 3318 binds nations, not suppliers or contractors. It addresses participating nations and NATO bodies for ratification and implementation, and separately states that "the partner nations are invited to adopt this STANAG"; the word "contract" does not appear in its own text. It becomes binding on a given nation through ratification, which NATO records in the NATO Standardization Document Database (NSDD): nations are "invited to examine their ratification of the STANAG and, if they have not already done so, advise the NSO of their intention regarding its implementation." Implementation is a separate, further step, reached only once "a nation has issued the necessary orders/instructions putting the details of the agreement into effect." Nations are separately "invited to report on their effective implementation of the STANAG in accordance with AAP-03", and partner nations are invited to report their adoption of it the same way. There is no NATO-wide compliance date printed in this cover; whatever date matters comes from a nation's own implementation timetable, or from a tasking or contract that invokes AAMedP-1.7.

How it's evaluated

STANAG 3318 describes no certification scheme and no audit. What it describes is nations reporting their ratification and implementation status to NATO for the record; the document never uses the word "certified" or "certification". Where an organisation's own accident-investigation procedures and training do get checked in practice, the assessor and the evidence required are set by whatever contract, tasking or government quality regime invokes them, not by this STANAG.

Standards it references

STANAG 3318 covers AAMedP-1.7, the Allied medical publication that carries the actual content on aeromedical aspects of accident and incident investigation. Its "Other Related Documents" also name STANAG 3531 (covered by AFSP-1.3), on safety investigation and reporting for military aircraft, missiles and UASs, and STANAG 7106 (covered by AAGSP-02), on breathing oxygen characteristics and supply couplings, both of which inform rather than bind through this agreement. It also names ICAO Annex 13, on civil aircraft accident and incident investigation, which sits outside our catalogue. Nations report their implementation of STANAG 3318 itself in accordance with AAP-03.

Put STANAG 3318 on a system that keeps the evidence

Documents, training, risks and evidence in one place, with the trail an auditor asks for.

How we help

STANAG 3318's own obligations fall on nations and NATO bodies: what changes on the ground is how a nation's aeromedical accident-investigation function documents and reports its work under AAMedP-1.7, not a product or a piece of software.

For an organisation supporting that function under a contract or tasking that invokes it, what ComplyTrain does for that kind of work in general is give it a single auditable place to hold the procedures and training records for the people who carry out investigation work, and the evidence trail, reviews, corrective actions, document control, that a government quality representative or a customer audit would ask to see.

ComplyTrain does not conduct aeromedical investigations, does not replace the qualified investigators AAMedP-1.7 requires, and does not determine whether a nation's implementation meets the publication. That is a matter for the nation's own investigation authority and AAMedP-1.7 itself.

Which STANAGs and Allied Publications actually apply to a given programme is set by the contract and the customer's quality clause, not by us. Browse the explorer to see what sits alongside STANAG 3318 and AAMedP-1.7, and talk to us about the evidence trail once you know which ones are in your contract.

Standards it references

Request access to this standard

Tell us how you need to work with STANAG 3318 and what you need from it. We will come back to you about what ComplyTrain can do.

Questions

Is STANAG 3318 mandatory?

Only where a nation has ratified and implemented it, and only where a tasking or contract invokes it. The cover names no NATO-wide compliance date of its own.

What is the difference between STANAG 3318 and AAMedP-1.7?

STANAG 3318 is the NATO ratification agreement; AAMedP-1.7 Edition B is the publication that actually sets out the points to be covered in an aeromedical investigation of an aircraft accident or incident. Ratifying STANAG 3318 is how a nation commits to implement AAMedP-1.7.

Can an organisation be certified to STANAG 3318?

No. STANAG 3318 describes nations ratifying and reporting implementation to NATO, recorded in the NATO Standardization Document Database. It describes no certification or audit scheme for an organisation or a product.

Does STANAG 3318 supersede an earlier edition?

Yes. This is Edition 8, and the document states plainly that it "supersedes the following document: STANAG 3318, Edition/Édition 7."

What ComplyTrain does

One system for the whole compliance programme. Start with the module you need most.

  • Forms & Follow-up

    Collect information the same way every time, and decide in advance what happens next.

  • Controls & Assurance

    Know whether your controls are operating, not just whether a policy says they exist.

  • Project Planner

    Turn the compliance work you already know about into a plan with owners, dependencies and dates.

  • Product Compliance

    Know what you can offer, and hold the evidence behind every configuration you offer it in.

  • Reporting & Analytics

    Eight built-in reports across every module, scheduled, delivered, and filed where the evidence lives.

  • Media Monitoring

    The sector news that matters to your organisation - read and rated by AI, and delivered as a scheduled digest in your own language.

  • Grants & Tenders

    AI reads the tender pack and pulls out the requirements, deadlines and rules - then helps you draft the response from your own approved content, with you reviewing every step.

  • Stakeholder/Vendor Management

    One current register of the suppliers and partners you depend on - each risk-assessed, re-assessing itself on schedule, and wired straight into your risk register.

  • Requirements Management

    See every requirement you face - across every standard, plus your own contracts and policies - traced to the documents, evidence and processes that satisfy it.

  • Risk Management

    Identify, score, treat and review your risks in one place - with AI to help anyone run a proper assessment, and a defensible trail behind every decision.

  • Training Management

    Assign training, prove it was understood, and hold the competence records an auditor asks for.

  • Document Control

    Draft compliance documents with AI, keep every version under control, and export them beautifully branded - all in one place.

  • Quality Management

    Audits, corrective actions, processes and approvals in one quality system, organised around ISO 9001.

Latest from ComplyTrain

  • Compliance in medical device manufacturing: an overview

    Medical device manufacturers operate under more regulatory pressure than almost any other sector outside pharmaceuticals. The rules govern how you design a device, how you make it, how you track it after it ships, and how you respond when something goes wrong.

Other standards in Air operations

  • AAEP-01AAEP-01 ground recharging of aircraft main batteries
  • AAEP-02AAEP-02 static grounding connections for aircraft and ground equipment
  • AAEP-05AAEP-05 aircraft tolerance to portable electronic devices
  • AAGSP-01AAGSP-01 nitrogen and replenishment equipment characteristics
  • AAGSP-02AAGSP-02 breathing oxygen and replenishment equipment characteristics
  • AAGSP-03AAGSP-03 breathable air characteristics for aircraft on the ground

Compliance work does not have to live in documents and spreadsheets

See ComplyTrain on your own processes in a 30-minute demo, with your quality or compliance lead.