ISO 9001:2015 + ISO 14001:2026 · $249 · Editable Word format
If you are certified to ISO 9001 and ISO 14001 but not to ISO 45001, this is your document.
It exists because the fully integrated variant is not the right answer for you. That one carries worker participation in cause evaluation, the hierarchy of controls at action selection, and a pre-implementation hazard assessment — three ISO 45001 requirements you do not have. A procedure that imposes obligations your standards never made is a procedure your own auditor will hold you to.
This is one procedure covering ISO 9001:2015 Clause 8.7 control of nonconforming outputs and Clause 10 in full, together with ISO 14001:2026 Clause 10 in full. Editable Word format, filled-in worked example, bracketed placeholders where values are yours to set.
The join that pays for it. A scrapped batch is a quality disposition and a waste stream at the same time. In two separate procedures nobody owns the handoff — the quality entry closes on the supplier issue, and the material goes into whichever skip is nearest. This procedure extends the scope at disposition, so the waste classification and the disposal route are determined by the environmental function before the material moves. There is an indicator in Section 10.0 that measures exactly that, and it is usually the first number to move after adoption.
What each standard adds that the other does not have. ISO 9001 contributes control of nonconforming output — a concept ISO 14001 has no equivalent for — and the requirement to update risks and opportunities when corrective action is taken, which is the only place in either standard where the corrective action loop touches the risk register. ISO 14001 contributes the significance test that ties the depth of response to the aspects register, mitigation of adverse environmental impacts as an obligation distinct from correction, and the compliance obligation chain running from determination through evaluation into correction. This procedure applies the union, with each requirement marked by the standard that provides it.
Appendix D is what you cannot easily assemble yourself. Eight genuine divergences between the two standards on this subject, what this procedure does about each, and what the alternative was — including the deliberate decision to omit the four ISO 45001 requirements, so that their absence reads as a decision rather than an oversight. Followed by nine decisions to confirm before adoption.
Everything in both single-standard templates, integrated into one document — 45 pages, editable Word format — plus:
Organizations certified to ISO 9001 and ISO 14001 and not to ISO 45001. Manufacturers, processors and service organizations with an environmental permit or a waste stream, running quality and environment through one management function. Consultants supporting clients through integration. If you are also certified to ISO 45001, take the integrated variant instead.
9001: 8.7, 10 · 14001: 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 |
| Integrated (9001 + 14001 + 45001) | $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, Q/EMS for ISO 9001 with ISO 14001, HSE for ISO 14001 with ISO 45001, and 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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