Start a free trial
Menu

STANAG 2347

STANAG 2347 medical warning tag

NATO nations and NATO bodies implementing the AMedP-8.8 medical warning tag scheme

STANAG 2347 is NATO's agreement committing member nations to implement AMedP-8.8, the Allied Medical Publication for the medical warning tag.

Edition
3
Published
2017-10-30
THIS DOCUMENT Agreement Holds requirements Organisation certificate Product or design assessed STANDARDIZATION AGREEMENT · EDITION 3 · 2017-10-30 STANAG 2347 MEDICAL warning tag STANAG 2347 is NATO's agreement committing member nations to implement AMedP-8.8, Edition A, the Allied Medical Publication for the medical warning tag. AGREEMENT STANAG 2347 The NATO agreement. The specification is not in this cover. WHERE THE REQUIREMENTS LIVE AMedP-8.8 AMedP-8.8 sets out the NATO Medical Warning Tag a member of NATO Forces with a significant medical condition wears, agreed by nations under STANAG 2347, with no certification schem. The requirements live in AMedP-8.8, not in STANAG 2347. Addressed to national authority. Puts AMedP-8.8 into force. The document describes a review cycle at least once every three years with the result recorded in the NSDD; it names no accredited or notified body and no schem. 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

What STANAG 2347 covers

STANAG 2347 is the NATO standardization agreement that gives force to AMedP-8.8, Edition A, the Allied Medical Publication for the medical warning tag. A STANAG is not itself a technical specification: it is the agreement by which NATO nations commit to implement one, and the tag's own content, covered in AMedP-8.8, sits in that publication rather than in this short cover. The stated interoperability requirement is "to have a description of significant medical conditions of wounded soldiers who are not able to communicate," with medical warning tags forming a complementary part of medical records. Read plainly, that means this STANAG covers the agreement to use a standard tag for that purpose - not the tag's design, colours, dimensions, or the medical conditions it lists, all of which belong to AMedP-8.8.

This is Edition 3, promulgated 30 October 2017. It supersedes an earlier edition of STANAG 2347.

Who ratifies it, and how it takes effect

The mechanism that matters here: a STANAG binds a nation, not a supplier. The agreement "has been ratified by member nations, as reflected in the NATO Standardization Documentation Database (NSDD)" and "is effective upon receipt and ready to be used by the implementing Nations and NATO bodies." Partner nations are only invited to adopt it. National ratification decisions are provided to the NATO Standardization Office and recorded in the NSDD; a supplier meets AMedP-8.8's tag scheme only where a contract or a tasking brings it into a programme, not because this STANAG exists on its own.

Implementation, reporting and review

Nations follow the recommendations set out in AMedP-8.8 and its annexes; this STANAG names no technical clause of its own. Beyond that, it asks nations to report on their effective implementation "using the form in Annex H to AAP-03(J)," and partner nations to report their adoption "using the form in Annex G to AAP-03(J)." The STANAG "is to be reviewed at least once every three years," with the outcome recorded in the NSDD, and a nation or NATO body may propose changes at any time through a standardization proposal to the tasking authority, processed at the next review. Oversight sits with the Military Committee Medical Standardization Board (MCMedSB) and its Medical Standardization Working Group; the custodian nation is Slovakia.

Related documents named in the cover

The cover names STANAG 1059 (letter codes for geographical entities), STANAG 2453, which itself covers AMedP-8.13 on dental and maxillo-facial treatment at Roles 1-3 medical support, and the World Health Organization's International Statistical Classification of Diseases, 10th revision, as other related documents. None of these is described as a binding requirement of this STANAG; they sit alongside it as related reading. STANAG 2347 itself is unclassified and free of charge - NATO's Standardization Document Database lists it, and we do not host a copy or sell it.

Put STANAG 2347 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 2347 and AMedP-8.8 describe an operational medical documentation scheme, not a management system: the actual work, completing and carrying a medical warning tag for a wounded soldier, sits in field medical handling, not in software. What that leaves to evidence is the paperwork around it: procedures that correctly reference AMedP-8.8 and this STANAG, training records showing medical personnel have been briefed on the scheme, and the trail an internal or customer audit asks for afterwards.

ComplyTrain holds that evidence as a modern, auditable system: version-controlled procedures, training records tied to named individuals and dates, and corrective actions when a gap turns up, all searchable when a higher headquarters or a customer's quality clause asks for it. It does not design or produce medical warning tags, does not record or assess a soldier's medical conditions, and does not replace the ratification and reporting nations carry out themselves through the NSO and the NSDD.

The applicable tier here, and whatever else it comes with, is set by the contract and the customer's quality clause. If you are working out what sits alongside STANAG 2347, the standards explorer covers the related NATO medical publications, and we are glad to talk through what that means in practice.

Standards it references

Request access to this standard

Tell us how you need to work with STANAG 2347 and what you need from it. We will come back to you about what ComplyTrain can do.

Questions

Is STANAG 2347 mandatory?

Not in general. It binds a nation once that nation ratifies it, and it reaches a supplier or a medical unit through a national order or a contract, not by existing on its own. Whether it applies to a given programme is set by the tasking or contract in front of you, not by the STANAG alone.

What is the difference between STANAG 2347 and AMedP-8.8?

STANAG 2347 is the agreement: the letter of promulgation, the ratification record, and the reporting and review machinery. AMedP-8.8 is the Allied Medical Publication itself, the specification for the medical warning tag that the STANAG gives force to. The STANAG is the cover; AMedP-8.8 is the content.

What edition is current, and what did it replace?

Edition 3, promulgated 30 October 2017. It supersedes an earlier edition of STANAG 2347.

Is ComplyTrain certified against this standard?

No. There is no accredited certification for STANAG 2347 or AMedP-8.8 to hold, and ComplyTrain does not claim one. What we support is the evidence trail around implementing and training against the scheme, at an informational level.

Who is the custodian of STANAG 2347?

Slovakia. The STANAG is supervised under the Military Committee Medical Standardization Board (MCMedSB) and its Medical Standardization Working Group.

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 Medical

  • AJMedP-1AJMedP-1 Allied joint medical planning doctrine
  • AJMedP-2AJMedP-2 medical evacuation doctrine
  • AJMedP-3AJMedP-3 medical intelligence doctrine
  • AJMedP-4AJMedP-4 Allied joint medical force health protection doctrine
  • AJMedP-5AJMedP-5 NATO doctrine for medical communications and information systems
  • AJMedP-6AJMedP-6 civil-military medical interface doctrine

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.