Why this exists
Most management review agendas were built from last year's agenda
Ask which clause a given section of your management review satisfies, and there is often no answer — because the agenda was assembled from what the last review covered, in the order it covered it. That works until the review meets an auditor.
The requirements an organization has never performed are precisely the ones a habit-built agenda cannot surface. If customer satisfaction was never reported, the agenda has no line for it. If nobody established audit objectives, no section asks for them. The gap is invisible from inside the document.
These toolkits invert that. Every input and every result the clause names gets its own numbered section, with the clause reference printed under the title. Where a section is MSI practice rather than a requirement, it says so — so an auditor can tell the difference, and so can you.
Each toolkit is a matched pair: a PowerPoint deck to present from and a Word minutes form to record into, generated from the same section list. Section 12 on the slide is Section 12 on the form. The presenter and the recorder are never on different items.
Start here
Choose by what your system is certified to
Pick the row that matches your certification scope. Combined-system toolkits are not two documents stapled together — they resolve every point where the standards diverge, and record which one governs.
| Your certification scope | Toolkit | Sections | Price |
|---|---|---|---|
| ISO 9001 only | ISO 9001 Management Review Tool Kit | 21 sections | $149 |
| ISO 14001 — transitioning to the 2026 edition | ISO 14001:2026 Management Review Tool Kit | 24 sections | $249 |
| ISO 45001 only | ISO 45001 Management Review Tool Kit | 27 sections | $149 |
| ISO 13485 — medical device | Medical Device ISO 13485 Management Review Tool Kit | 23 sections | $149 |
| ISO 7101 — healthcare | ISO 7101 Management Review Tool Kit | 26 sections | $149 |
| AS 9100 D — aerospace | AS 9100 D Management Review System | 23 sections | $149 |
| ISO 9001 + ISO 13485 | Combo Medical Device ISO 13485 and ISO 9001 | 32 sections | $149 |
| ISO 9001 + ISO 14001 | ISO 9001 and 14001:2026 Management Review Tool Kit | 29 sections | $349 |
| ISO 14001 + ISO 45001 (HSE) | ISO 45001 and 14001:2026 Management Review Tool Kit | 30 sections | $249 |
| ISO 9001 + ISO 14001 + ISO 45001 (IMS) | IMS Management Review Toolkit | 33 sections | $349 |
| Not certified — building the discipline first | General Purpose Management Review (Path to Quality) | 25 sections | $149 |
Single-standard toolkits
One standard, one review
ISO 14001:2026
Twenty-four numbered sections built to the 2026 edition, with a ten-row comparison against 2015 — what moved and what each change means for your record. Clause 9.3 is now split into three subclauses, outputs became results, and Clause 9.2.2 a) asks for an audit objective the 2015 edition never required.
View the ISO 14001:2026 toolkitISO 45001
Twenty-seven numbered sections. ISO 45001 is the only standard in this family that requires the results of the review to leave the room — top management must communicate them to workers and their representatives, and the toolkit carries a five-column log recording what went to whom, by what means, when, and why anything was judged not relevant.
View the ISO 45001 toolkitISO 7101 — Healthcare
Twenty-six numbered sections. ISO 7101:2023 carries the longest list of mandatory review inputs of any ISO management system standard, and six of them exist in no other standard — health indicators, patient safety, waste management, internal finances and external funding, accessibility of services, and information owed to stakeholders under agreement.
View the ISO 7101 toolkitISO 9001
The quality management review, presented as top management needs to see it. A deck and a minutes form covering the key requirements and the data that has to be reported, so the record demonstrates how seriously the organization takes the system it is reviewing.
View the ISO 9001 toolkitISO 13485 — Medical Device
The device management review, where the clause sits at 5.6 inside Management Responsibility rather than at 9.3. Built to take the guesswork out of what a professional device review has to present. Already ISO 9001 certified? The combined edition is the better fit.
View the ISO 13485 toolkitAS 9100 D — Aerospace
The aerospace management review system, covering the review requirements an AS 9100 D quality management system carries. A deck to present from and a minutes form to record into.
View the AS 9100 D systemGeneral Purpose — Path to Quality
For organizations new to the standards that want the discipline before the certificate. Includes the educational material alongside the deck and minutes tracker, and prompts to insert your own data. Where a concept is not yet in place — customer satisfaction measurement, corrective action — the review records that as the finding and sets the goal.
View the General Purpose toolkitCombined-system toolkits
Two or three standards, one review
An integrated agenda is not the longest of its parts. Requirements exist in one standard and not the others, and the asymmetry runs in every direction — which is why building the combined agenda from whichever standard you know best drops the requirements the others carry alone. Each combined toolkit carries an appendix recording every divergence, which standard governs it, and the alternatives considered and rejected.
ISO 9001 + ISO 13485
Thirty-two numbered sections built from 9.3 and 5.6 together. A device organization building from ISO 13485 alone misses three ISO 9001 inputs; one building from ISO 9001 alone misses six ISO 13485 requirements. Since February 2026, ISO 13485:2016 is incorporated by reference into 21 CFR Part 820 — and the exemption that shielded management review records from routine FDA inspection was not carried forward.
View the device combo toolkitISO 9001 + ISO 14001:2026
Twenty-nine numbered sections. The most common dual certification in North America, and the one where the 2026 revision does the most damage to a habit-built agenda: Clause 9.2.2 a) now requires an audit objective, and in a single integrated audit programme that requirement reaches the quality audits too — not just the environmental ones.
View the ISO 9001 and 14001:2026 toolkitISO 14001:2026 + ISO 45001
Thirty numbered sections, fourteen divergences resolved. Both standards apply to the whole organization at all times, so there is no scope determination to fall back on — every difference has to be decided rather than partitioned. Including the one most organizations have not worked out: in one audit programme, the ISO 14001:2026 requirement for audit objectives reaches your safety audits too.
View the HSE combo toolkitISO 9001 + ISO 14001:2026 + ISO 45001
Thirty-three numbered sections and the hardest of the set to assemble alone. Twelve requirements exist in one of the three and not the others. Build from ISO 9001 and you drop worker consultation, incidents and compliance evaluation; build from the environmental and safety agendas and you drop customer satisfaction, external providers and risk-action effectiveness.
View the IMS toolkitInside every toolkit
What you get
Every toolkit on this page is built to the same architecture — numbered sections anchored to the clause each one satisfies, and the same set of supporting pages. Each is delivered as one .pptx and one .docx, fully editable, with no protection and no macros.
A presentation deck
What you present from. A numbered badge, the clause reference, and a preparation prompt on every section slide.
A Word minutes form
The record the clause requires, with every section anchored to the requirement it satisfies.
One shared spine
Deck and form generated from the same section list, so the presenter and the recorder are never on different items.
Worked examples
Example slides showing completed data, each marked as example data to replace. Native editable charts, not images.
Terms used
Plain-language explanations of every term carrying a specific meaning in the standard, with the clause where each is defined.
Before you hold this review
Each section mapped to the record that feeds it, and what to do if you do not have it — so you find out while preparing, not at audit.
Document control throughout
Company name placeholder, period covered, template revision date and review date, marked internal use and proprietary on every slide and page.
An appendix of divergences
On the four combined editions: every point where the standards differ, which one governs, the alternative not taken, and the decisions to confirm before adoption.
Stated plainly
What these toolkits do not do
They do not make you compliant
A toolkit records what the clause requires, with every entry traceable to it. Compliance depends on the management system the review is reviewing, not on the document that reports it.
They do not create the records they draw on
A management review cannot manufacture an aspects register, a hazard identification, a compliance register, or a set of health indicators that do not exist. Where one is missing, the toolkit captures that as the finding — which is the honest answer rather than a workaround.
A record is not a procedure
ISO 13485, 5.6.1 requires both a documented procedure and a record. These toolkits are the record. The procedure comes from MSI's Leadership and Commitment procedure template.
The worked examples are fictional
Every example uses a fictional organization created by MSI for illustration, marked as such throughout and intended to be replaced with your own data before the review is held.
Works alongside
The rest of the system
ISO 14001:2026 Transition Course
The management review is not the last step of a transition — it is the specification for one. This course covers every clause change, the new Clause 6.3, and the register updates the 2026 edition requires. First module free.
View the transition courseISO Procedure Templates and Guides
The procedures that produce the data a management review reports. Thirteen procedure families and 100+ templates across ISO 9001, 13485, 14001:2026, 45001 and 7101, written to one architecture so the set interlocks — including the Leadership and Commitment procedure the review record depends on.
Browse the template libraryISO 9001 Internal Auditing — 2 Day
Internal audit results are a mandatory input to every management review on this page, and a review is only as good as the audits feeding it. Two days on planning, interviewing, sampling, and writing findings that drive corrective action rather than sit in a folder.
View the internal auditing courseNot sure which one
Tell us your certification scope and we will tell you which toolkit fits
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