- Document reviews, revisions and approval routing
- Evidence collected against every control cycle
- The internal audit programme, planned and conducted
- Findings followed up to verified closure
- The risk register, maintained on its review dates
- Preparation for every certification visit
We run your compliance programme.
You keep the decisions.
A named compliance manager carries the documents, the evidence, the internal audits and the risk register, on a schedule, against every standard, regulator and lender you answer to. When the auditor sits down, your team stops searching and starts showing.
We publish no outcome figure we cannot evidence. Reference calls are arranged once a client has agreed to take them.
A management system that is current on any ordinary day.
Most compliance vendors sell you a place to do the work. We do the work. The platform is where it lands, and where you check it whenever you want to.
- Every decision. Policy, scope, risk appetite, approvals
- The certificate and the relationship with your certification body
- Your data, in a workspace you own and can export in full
- Your independence. We do not certify you and never will
- Your people, doing the work they were hired to do
You are buying an outcome.
If the system is not current on the day someone asks, we have not delivered, whatever the software happens to show. That is the standard, and it is the one written into the engagement letter.
They ask for the calibration cert for MD-04.
Same question, two operating models. Below is the audit moment compliance teams know by heart, and what changes when the records are linked.
Three drives, two days, one apology.
- 1QA Lead opens the shared drive. The calibration certs folder has 41 PDFs. None of them are named MD-04.
- 2She emails the previous maintenance manager, who left in November. No response by lunch.
- 3The auditor asks for the linked CAPA. There is one, somewhere. Last accessed in a Word doc by someone who is on leave.
- 4Two days later, the cert is found in a sub-folder named "old_finals_v2_USE". The audit team writes an OFI for retrieval delays.
Search, open, move on.
- Calibration cert MD-04 v3evidence · valid until Apr 17, 2027
- QMS-PROC-008 §4.2document · monthly calibration program
- CAPA-2026-0098 (closed)finding · MD-04 drift, last cycle
Three linked records on screen in under five seconds. The auditor sees the cert, the policy that owns the cadence, and the CAPA that proved the program works. Audit pack exports as one PDF.
The same work, carried differently.
Nothing in the middle column is a criticism. It is what a competent team does when compliance is the seventh thing on a list of six.
Someone remembers, or nobody does. Versions drift across drives and inboxes.
Review dates are tracked. We prepare the revision and route it for approval.
Gathered in a rush before the auditor arrives, from whoever still has the file.
Filed as the work happens, against the control it proves.
Squeezed in when the calendar allows, often late in the cycle.
Programmed a year ahead and run to that plan.
Noted, assigned informally, revisited next cycle in much the same words.
Owner, due date, root cause, verification, closed and evidenced.
A spreadsheet refreshed before the board paper, rated once and rarely revisited.
Each risk carries a cause, a consequence, the control that reduces it and a review date.
Assembled by hand before each meeting from whatever can be found in time.
A standing monthly report, drawn from the same records the auditor will open.
Six weeks of preparation, most of it reconstruction.
An ordinary week. The pack already exists.
The difference is cadence. The right column is not harder work. It is the same work done on a schedule somebody owns, which is exactly the thing a busy organisation cannot reliably supply.
Quality, safety, security, environmental, food, pharma, privacy, regional. New standards ship as installable modules, cross-mapped at the requirement level.
Browse module storeEight workflows,
and we run all of them.
Eight workflows. They feed each other. Nothing crosses a spreadsheet boundary on the way to the audit folder.
Decide what applies. Defend why.
Policies that don't fall out of date.
Map what you do to what's required.
Files that show up when the auditor asks.
Run the audit. Get a real report at the end.
Close the loop with a different person.
Linked to controls. Linked to action.
Decisions, on the record.
- 10:14Approve scope reduction · KEBS KS 2466Exec
- 10:21Allocate budget · 4 calibration unitsQM
- 10:33Defer SA8000 onboarding to Q4Board
- 10:48Open CAPA on supplier audit overdueQA
Every standard you answer to, already loaded.
When ISO 9001 ships its next amendment, your consultant won't email you a 60-page PDF and a Word table of what changed. You get a version diff. You review it. You upgrade.
- 8.2.4 · Customer property · visit logs
- 9.1.3 · Trend analysis on complaints
- 10.3 · Continual improvement evidence
- 7.5.3 · Now requires retention metadata
- 8.5.1 · Tightens production change control
- 9.2 · Internal audit competence rules
Calibration cadence for metal detectors on Line 3 is monthly, per QMS-PROC-008 §4.2 and the FSSC 22000 prerequisite program. Next due: Apr 18.
- · Owner: J. Otieno (Maintenance)
- · Linked control: CTRL-027 · linked finding: Q1-INT/03
- · Verifier: K. Mbeki (different from owner)
- · Effectiveness review: 2 cycles after closure
AI that an auditor can trust.
Every answer points at a record in your tenant. Anything that writes data waits for a human to click Approve. The transcript lands in your audit log next to the change itself.
- The auditor role doesn't see what the admin sees. Retrieval respects it.
- Citations resolve to live records, not URLs that rot.
- Write actions stage as proposals. A named person approves them.
- Every prompt, source, and decision is recorded for the next audit.
You speak IMS. Your regulator speaks GRC. We work in both.
Quality leaders talk scope, CAPA, and management review. Risk and security leaders talk controls, attestations, and remediation. Same workflow. Different label.
One tenant. One audit log. Whichever language your team uses on the morning of the assessment.
Seven tests. Run any of them without warning us.
We would rather be measured than described. Every test below is checkable by you, on any working day, without asking us to prepare anything. If preparing it is required, the system is not running, and running it is the work you were trying to hand over.
We are early, and we would rather say so than invent a logo wall. Named references are introduced on request once a client agrees to it, and we will tell you plainly which parts of the service they use. Until then, judge the model on the tests, and on the working session.
- 01The certificate holds
Visits close with no major nonconformity, and minors are verified closed before the next one.
- 02Any question is answered from a record
Name any control. Owner, frequency, last evidence and date, in under a minute, with no notice.
- 03Findings close and stay closed
Owner, due date, recorded root cause, verified by someone other than the owner.
- 04Evidence exists before it is asked for
The pack for the next visit is assembled continuously, against the control it proves.
- 05Your board sees it without asking
One monthly report from live records: what moved, what is late, what needs your decision.
- 06The month does not change the quality
The same review runs the same way whoever is on it, because the system will not let a step be skipped.
- 07The system survives a resignation
The register, the evidence and the decision history stay current and legible to whoever arrives next.
The compliance trail is the product.
The same controls that keep your data safe are the ones the certification body asks about during a vendor review. Honest answers, on one page.
Your tenant is yours
Your records never sit next to another customer's records. The same query, run by a different tenant, returns nothing.
Auditor doesn't see admin
Per-role and per-site boundaries on every read. The contractor working at the Mombasa plant can't see the Lagos plant.
No one approves their own work
Authors can't approve their own documents. CAPA verifiers can't be the CAPA owner. The platform refuses, not the policy.
Every change is on the record
Approvals, scope changes, evidence acceptances, AI actions. Append-only log with actor and prior state. Export to CSV.
No public file links
Evidence is reached through time-limited signed URLs. TLS in transit, AES at rest. The cert PDF you shared in November isn't reachable today.
Your data lives where you say
EU, US, or Africa. Pick once, the tenant stays there. Cross-region replication is opt-in.
Bring your real scope. We will run a month of it in front of you.
Bring three policies, a recent audit report, and one CAPA that's been open too long. We index your records into a scoped tenant and run the workflow your team would run on Monday. Forty-five minutes.
- A scoped tenant loaded with the standards you actually run.
- That open CAPA, walked from finding to verification.
- A two-page brief on which modules to install first.
- An honest no, if it's not a fit.
