Start a free trial
Menu

AMedP-8.7

AMedP-8.7 first aid kits and emergency medical care kits

Nations assembling and issuing Individual, Vehicle and Special Purpose First Aid Kits, and the trained personnel who carry and use them

AMedP-8.7 sets the minimum contents of the first aid and emergency medical kits NATO nations issue, agreed under STANAG 2126, with assembly and issue left to national discretion.

Edition
A
Published
2018-03
THIS DOCUMENT Agreement Holds requirements Organisation certificate Product or design assessed ALLIED MEDICAL PUBLICATION · EDITION A · 2018-03 AMedP-8.7 Firstaid dressings, first aid kits and emergency MEDICAL care kits AMedP-8.7 sets NATO's minimum first aid and emergency medical kit contents for Individual, Vehicle and Special Purpose Kits and Annex A's Emergency Medical Care Kits, agreed under . AGREEMENT STANAG 2126 The agreement that puts this publication into force. WHERE THE REQUIREMENTS LIVE AMedP-8.7 AMedP-8.7 sets NATO's minimum first aid and emergency medical kit contents for Individual, Vehicle and Special Purpose Kits and Annex A's Emergency Medical Care Kits, agreed under . A supplier meets AMedP-8.7 when a contract or national instruction names it, usually via STANAG 2126. Addressed to national authority, operator. Covered by STANAG 2126. The document sets minimum kit contents and leaves assembly, issue and any supplementation to national discretion; it names no certification, audit or inspection. Reaches a supplier when a contract, tender or national instruction names it. Nobody is certified against this document. Nations report ratification; they do not issue a company certificate.

What it is

What AMedP-8.7 covers

AMedP-8.7 is the NATO Allied Medical Publication that fixes the minimum contents of the first aid and emergency medical kits NATO forces carry. It covers four kit types: an Individual First Aid Kit "is recommended to be carried by all military personnel"; a Vehicle First Aid Kit carried in military vehicles; special purpose kits that nations develop for environments such as jungle, snake-bite risk, survival, Special Operations Forces, or air and naval operations; and, in Annex A, Emergency Medical Care Kits carried by "trained and credentialed medical personnel above the level of combat life saver," described in the document as medics, nurses and doctors, working forward of any medical treatment facility. The document states plainly that "the following kits and their items are the minimum required for essential first aid of NATO Forces and will be provided at appropriate levels," and that nations may supplement the number of kits and items at their own discretion.

How it comes to bind

Nations record their agreement to use AMedP-8.7 in STANAG 2126: "the agreement of nations to use this publication is recorded in STANAG 2126." AMedP-8.7 is the technical content; the STANAG is what commits a nation to it, and a nation can ratify with a reservation, as several have here. The current edition, Edition A, Version 1, was approved by the nations in the Military Committee Medical Standardization Board and became effective on receipt in March 2018. For an organisation, the practical route in is not the STANAG itself: it is whatever a nation's own procurement or kit-assembly requirement specifies, since AMedP-8.7 addresses nations rather than suppliers directly.

What the chapters set out

Chapter 1 covers the Individual First Aid Kit and the Vehicle First Aid Kit. Both are to be "assembled and issued at national discretion," with all military personnel expected to be "adequately trained in the proper wear and maintenance of the kit, and be properly trained in the application and use of all components," and potency dated materiel is to stay "held under medical supervision until issue is required." The Vehicle First Aid Kit carries "the same equipment as the individual kit, in a sufficient amount in accordance with national regulations." A separate clause recommends that nations develop special purpose kits, such as jungle, snake-bite, survival, Special Operations Forces, or air and naval kits, "in accordance with national requirements."

Annex A covers Emergency Medical Care Kits, carried by trained and credentialed medical personnel working above combat life saver level. Their contents depend on "the competency of the personnel, operational environment and transport platforms," and the annex expects the kit to follow recognised battlefield trauma-care principles, which it names as TCCC. Nations are told to "review these medical kits in light of their own requirements and tailor them to the specific operations." This page does not reproduce the item-level contents of any kit: that is exactly the testable detail the document itself leaves to a nation's own kit specification.

Where nations differ

The promulgation record lists formal reservations from Canada, Czechia, France, the UK, the Netherlands, Norway and the Slovak Republic, each stating where its own kit provision departs from the common baseline. That is the document's own mechanism for a nation to record a difference, not a sign of non-compliance. The UK's reservation separately states that "British Standard BS8599-2 will continue to be the baseline standard for GBR Vehicle First Aid Kits (V-FAKs)," a civil, UK national standard the document does not otherwise reference, kept alongside AMedP-8.7 rather than replaced by it.

Put AMedP-8.7 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

AMedP-8.7 is an operational document, not a management-system standard, and the substantive work of assembling, issuing and maintaining first aid and emergency medical kits happens inside a nation's own medical and logistics services, not in software. Where ComplyTrain fits is the evidence trail around that work: the procedure a unit writes for how its kits are assembled, issued and checked, including how potency dated materiel is monitored and replaced before issue; the training record showing personnel have been trained in the wear, maintenance, application and use of their kit's components; and the record of any national or unit-level variation from the common baseline, kept alongside the reasoning for it, the same way AMedP-8.7 itself records a nation's reservations.

What ComplyTrain does not do: it does not assemble, supply or manufacture first aid dressings, kits or their components, and it does not make the clinical decisions about what a casualty needs or how a kit is used in the field. Which items go into a kit, and how a reservation against the baseline is justified, is set by national medical authorities and NATO's own standardization process, not by this page. The standards explorer shows what else sits alongside AMedP-8.7, including STANAG 2126, and we are glad to talk through what a specific tender or kit-assembly requirement is asking for.

Request access to this standard

Tell us how you need to work with AMedP-8.7 and what you need from it. We will come back to you about what ComplyTrain can do.

Questions

Is AMedP-8.7 mandatory?

It binds through STANAG 2126, the NATO agreement recording nations' agreement to use this publication. A nation can ratify with a reservation, and several have; assembly and issue of the kits themselves are left to national discretion, so there is no single answer beyond what a nation's own regulations or a specific contract or tender require.

Can a kit or a supplier be "AMedP-8.7 certified"?

No. The document describes no certification, audit or inspection scheme of its own. Kit composition, assembly and issue are matters nations decide, and where practice differs from the baseline, the document's own mechanism is a recorded reservation at promulgation, not something a third party assesses or certifies.

What is the difference between the Individual First Aid Kit and the Emergency Medical Care Kit?

The Individual First Aid Kit "is recommended to be carried by all military personnel" and assembled at national discretion. The Emergency Medical Care Kit, covered in Annex A, is carried by trained and credentialed medical personnel above the level of combat life saver, such as medics, nurses and doctors, and its contents depend on their competency, the operational environment and the transport platform.

Why do some nations' kits look different from the common baseline?

AMedP-8.7 allows this by design. Several nations, including Canada, Czechia, France, the UK, the Netherlands, Norway and the Slovak Republic, recorded formal reservations at promulgation setting out where their own kits differ from the common minimum, and the document treats a recorded reservation as the normal route for a national variation, not as non-compliance.

Does AMedP-8.7 relate to civil standards like British Standard BS8599-2?

Only through one nation's reservation. The UK's reservation states that "British Standard BS8599-2 will continue to be the baseline standard for GBR Vehicle First Aid Kits (V-FAKs)." AMedP-8.7 does not otherwise reference BS8599-2 or any other civil dressing or kit standard.

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.