Skip to content

Zero Manual
Compliance Work.

Pio captures your operations and maps them to ISO clauses automatically. Audit-ready documentation builds itself while your team works — no forms, no checklists, no after-the-fact write-ups.

Let's Talk
What Pio Produces

Audit-Ready Output

01

ISO-Ready Audit Reports

Pio automatically structures your field data into audit-ready reports mapped to ISO clauses. When the auditor arrives, your evidence is already organized — timestamped, traceable, and exportable.

Mapped to ISO 9001, 45001, and custom frameworks
One-click PDF export for external auditors
ISO Compliance Report
Audit Period: Q1 2026
ISO 9001:2015 — Clause 8.5 Production & Service Provision
Process DocumentationPASS
42 procedures recorded with timestamped evidence
Corrective ActionsPASS
3 non-conformances identified, all resolved within SLA
Training RecordsPASS
100% onboarding sessions captured with video proof
Equipment CalibrationPASS
Pre-shift checks logged automatically for 28 consecutive days
Incident LogOPEN
1 open item — lockout procedure deviation on Line B
Report auto-generated from Pio capture data — no manual entry
Export PDF
02

Full Procedure Traceability

Every documented SOP is indexed with capture counts, operators, and last-recorded dates. Auditors can see at a glance which procedures have evidence — and drill into any one.

Process Documentation

ISO 9001:2015 — Clause 8.5.1 Control of production and service provision
PASS
Evidence Summary

42 procedures recorded across 28 working days

Coverage

100% of documented SOPs have at least one recorded instance

Recorded Procedures
SOP-101Machine Startup & Pre-Run Checks
12 capturesJ. MoreauApr 1
SOP-204Mould Changeover & Lockout
8 capturesA. DuvalMar 31
SOP-112Batch Quality Inspection
9 capturesM. BernardApr 1
SOP-305PPE Verification at Zone Entry
28 capturesAll operatorsApr 1
SOP-410End-of-Shift Equipment Shutdown
11 capturesJ. MoreauMar 31
Each procedure links to timestamped photo and video evidence — click any row to view full capture history
03

Step-Level Evidence

Pick any procedure and see exactly what happened — each step verified with timestamped photo evidence and operator attribution. This is what an auditor sees when they click into a row.

SOP-112

Batch Quality Inspection

Visual and dimensional inspection of each production batch before release. Operator verifies surface finish, dimensional tolerances, and labelling against the reference standard.

PASS
Revision

Rev. 3.1

Frequency

Every batch

Avg. Duration

4 min 12 s

Total Captures

9

Procedure Checklist
1
Retrieve batch sample from production line output tray
2
Visual check — inspect surface for cracks, burrs, or discoloration
3
Dimensional check — measure 3 critical dimensions with caliper against SOP tolerance table
4
Label verification — confirm batch number, date code, and operator ID match the production order
5
Log result in quality register and return sample or escalate to supervisor if out of tolerance
Captured Evidence
09:32Apr 1Step 1

Sample retrieved from Line A output tray — Batch 041

M. Bernard
09:33Apr 1Step 2

Surface inspection under task light — no defects detected

M. Bernard
09:34Apr 1Step 3

Caliper measurement on critical dim. #1 — 24.98 mm (tol. 25.00 ± 0.05)

M. Bernard
09:35Apr 1Step 4

Label match confirmed — Batch 041 / Date 2026-04-01 / Op. MB

M. Bernard
09:36Apr 1Step 5

Quality register updated — batch released for packaging

M. Bernard
All 5 steps verified with photo evidence — audit trail complete
Inspection ResultPASS