Primary Source
A brief from The Mender-Haüs Corporation
The month in one line
ISO 14001:2015 is already gone, and most calendars have not caught up
Not “being replaced.” Withdrawn. ISO moved the 2015 edition to stage 95.99 on 15 April 2026, which is the code for withdrawal of an International Standard, and ISO 14001:2026 stands in its place. Every internal audit checklist, procedure and clause cross-reference written against the 2015 text now points at a document that no longer exists.
Meanwhile ISO 9001 is due this month, and a good deal of what is being published about both is guesswork presented as fact. What follows is only what the issuing bodies themselves have put in writing, with the stage codes so you can check it.
Item one
Where the four standards actually stand
| Standard | Status at source | Transition period |
|---|---|---|
| ISO 14001Environmental | 2015 edition withdrawnISO stage 95.99, 15 April 2026 · replaced by ISO 14001:2026 | Running. Set by each accreditation body, not by ISO — confirm the date your own certification body works to. |
| ISO 9001Quality | 2015 edition at stage 90.92, “to be revised”since 16 November 2023 · new edition expected September 2026 | Not announced. Any specific end date you have been quoted is somebody's estimate. |
| ISO 45001Health & safety | 2018 edition at stage 90.92revision at draft international standard stage | No publication date. Treat any year you see quoted as speculation. |
| RC14001Responsible Care | 2026 technical specification publishedRCMS is at its 2023 edition | Set by the American Chemistry Council and its accredited certification bodies. |
A note on the sector schemes
Two of these are not standalone standards at all. RC14001 folds Responsible Care into the ISO 14001 structure, and IATF 16949 is applied together with ISO 9001 rather than instead of it. In both cases an ISO standard is the foundation and the sector scheme is built on top of it.
That relationship is structural, and it carries a consequence worth planning around: a scheme cannot keep pointing at a superseded edition of the standard underneath it. When the base moves, the scheme follows. RC14001 has already made that move. IATF 16949 has not yet, and the reason is visible in the row above — ISO 9001 has not published.
So the relationship is certain and the calendar is open. If you hold IATF 16949, the ISO 9001 edition landing this month is your event too, one step removed.
Item two
Global ACI replaced IAF and ILAC — and asks nothing of you yet
On 1 January 2026 the Global Accreditation Cooperation Incorporated became operational, taking over the roles of both the International Accreditation Forum and the International Laboratory Accreditation Cooperation. One body now where there were two.
What the published documents say, in order:
- Existing accreditation documents remain valid. Anything issued before 1 January 2026 stays valid until an administrative action occurs — renewal, re-issue, a scope change, or a change to the accredited legal entity.
- The legacy marks remain valid and are recognized as equivalent to the Global ACI MRA Mark through the transition.
- The new mark is not yet authorized for use. A formal decision on authorization was scheduled for October 2026.
- There is no single global switch date. Each economy transitions when the mark is legally available there and the Secretariat issues formal notification. From that point, new, renewed, re-issued or amended accreditation documents must carry the new mark.
- The anticipated end date for the legacy marks is 1 January 2029, or later if regulatory or market considerations require it.
At the time of writing, nothing. Your certificate is unaffected. You do not need it reissued, you do not need to reprint stationery, and you do not need a project. If someone offers to sell you a Global ACI transition, a fair question is which clause of Global ACI MRA-006 obliges you to act — and the honest answer today is none.
Where it will matter is at your next renewal or re-issue after your accreditation body is notified, and in how the mark appears on certificates and in your own marketing after that. Worth a diary note, not a budget line.
Item three
The transition work nobody budgets for
Reading a revised standard takes an afternoon. Aligning a mature management system to it does not, and that is where transition programs run late.
A system that has been certified for a decade carries procedures, forms, registers, competence matrices and audit checklists all written against the previous edition and cross-referenced to its clause numbers. None of that is difficult. All of it is finite. It is almost always discovered later than it should have been — most often in the week the certification body confirms the transition audit date.
The second thing that costs money is subtler: reading a revised requirement as equivalent to the old one when the emphasis has moved, or as a much larger change than it is and building work nobody needed. Both are cheap to correct in a review and expensive to correct in a finding.
Next issue
October
What ISO 9001:2026 actually changed, once the published text can be read rather than guessed at — and whether the Global ACI mark authorization decision landed on schedule.
Checked against
- ISO Online Browsing Platform — standard status and stage codes for ISO 14001:2015, ISO 9001:2015 and ISO 45001:2018.
- Global ACI, Frequently Asked Questions, and Global ACI MRA-006, Use of the MRA Mark by Accreditation Bodies and Claims of Accreditation Status, v1.0.
- American Chemistry Council, RC14001:2026 Technical Specification, and the RCMS:2023 Technical Specification.
Every date in this brief was checked against the issuing body's own document on 6 September 2026. Where a thing has not been decided, this brief says so rather than estimating. This is commentary on published documents and is not legal advice.
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