ISO 9001:2015 + ISO 14001:2026 + ISO 45001:2018 · $249 · Editable Word format
Three standards, three clause structures, one corrective action register that most integrated management systems never actually integrate. What usually exists instead is one procedure written from the quality side, with environmental and safety findings routed into it and the requirements those standards add quietly missing.
This is one procedure covering ISO 9001:2015 Clause 8.7 and Clause 10, ISO 14001:2026 Clause 10, and ISO 45001:2018 Clause 10 in full. Editable Word format, filled-in worked example, bracketed placeholders where values are yours to set.
What each standard adds that the others do not have. ISO 9001 contributes control of nonconforming outputs — a concept neither of the other two has — and the requirement to update risks and opportunities when corrective action is taken, which neither of the other two requires. ISO 14001:2026 contributes the significance test tying action to environmental impact, and the compliance obligation chain running from determination through evaluation into correction. ISO 45001 contributes incidents as a category, mandatory worker participation in cause evaluation, the hierarchy of controls at action selection, the pre-implementation hazard assessment, the distribution obligation, and five specific continual improvement requirements including culture.
This procedure applies the union, taking the stricter of each as the house standard, and marks which standard drives each requirement inline so nothing reads as arbitrary. The parts that apply to only one system are scoped rather than removed.
Appendix D records every divergence and every decision. An integrated procedure carrying three standards has more integration decisions in it than any single-standard document, and none of them are visible from reading the procedure itself. Appendix D is where they live, with the alternative stated for each, followed by the decisions to confirm before adoption.
Everything in the three single-standard templates, integrated into one document — 51 pages, editable Word format — plus:
Management representatives, IMS managers, and consultants at organizations certified to ISO 9001, ISO 14001, and ISO 45001. Particularly useful for organizations transitioning to ISO 14001:2026 who are rebuilding the improvement process anyway, and for anyone maintaining one procedure that claims to cover three standards but was written from one.
9001: 8.7, 10 · 14001: 10 · 45001: 10
| Variant | Price |
|---|---|
| ISO 9001 | $149 |
| ISO 13485 | $149 |
| ISO 14001:2026 | $149 |
| ISO 45001 | $149 |
| ISO 7101 | $149 |
| Device (9001 + 13485) | $249 |
| HSE (14001 + 45001) | $249 |
| Q/EMS (9001 + 14001) | $249 |
Both, and that is deliberate. It is written as a filled-in worked example so you can see what each element looks like when done properly, with bracketed placeholders wherever a value is genuinely yours to set — severity thresholds, roles, systems, intervals, retention periods. You are editing a working document rather than filling in a hollow outline.
Editable Microsoft Word (.docx), with a PDF copy. Where a process interaction map is included, it ships as an editable SVG alongside the embedded image. Adapt it, rebrand it, adopt it into your document control system. Yours to use.
A procedure does not pass an audit; an organization does. What this gives you is a procedure that addresses every requirement of the clause with a named owner and a named record, and that describes a process people can actually follow. Conformity is demonstrated by implementation and evidence — a perfect document over an operation that ignores it is still a finding. Unfilled placeholders are unmet requirements, so fill them.
No. Each covers the improvement clause of its standard in full, plus control of nonconforming output where the standard has such a clause. They are one procedure in a management system, and they reference the neighboring processes — document control, internal audit, complaint handling, risk management, management review — rather than replacing them.
Correction addresses the thing in front of you: scrap it, rework it, contain it, tell the customer. Corrective action removes the cause so it does not happen again. Every standard in this family requires both, and treats them as separate obligations. The common failure is one form doing both jobs, which lets a disposition record close a finding without any cause ever being examined. These templates keep them as two records with a stated trigger between them, which is usually the single biggest change an organization makes when adopting one.
A form captures what happened. A procedure decides what happens next — which findings get a cause analysis and which do not, who is allowed to decide, how long the organization has, what evidence closes it, and what happens when the check fails. Most systems have a good form sitting on top of an unstated process, which is why closure rates look healthy while the same findings keep coming back.
Every cross-reference is in a table at the back rather than baked into the body text, precisely so you can renumber without unpicking the procedure.
Take the template for the standard you are certified to. If you run more than one management system through one improvement process, take the matching combined variant — Device for ISO 9001 with ISO 13485, HSE for ISO 14001 with ISO 45001, Integrated for all three of quality, environment, and safety. If you are unsure, the free Nonconformity and Corrective Action Maturity Check will show you where your current process actually sits before you spend anything.
Yes. Call Management Systems International at 760-434-9141 to schedule a planning session.
MSI is a veteran-owned, woman-owned ISO consulting firm founded in 1998. Diana Lynn has 28 years of experience, has supported more than 80 organizations through successful ISO certification, has attended more than 200 certification and surveillance audits, and has trained more than 600 professionals across manufacturing, technology, medical device, government, healthcare and other regulated industries.
Questions before you buy? Call 760-434-9141.
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