01 / 05Photo to formVISION AI
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ISO 17025 Audit App
Plan, run, and close audits of a testing or calibration laboratory against ISO/IEC 17025 from any phone, tablet, or laptop. InspectWrk turns the standard's requirements into a mobile audit, captures evidence against each clause, records findings and nonconformities, assigns corrective actions with owners and due dates, and generates the audit report. It works offline and rolls findings up across the laboratory.
- Key checks
- 9
- Platforms
- iOS + Android
- Works
- Offline
Template aligned to ISO/IEC 17025:2017, the laboratory's own management system documentation and your accreditation body and applicable requirements.
ISO AuditPlant 2 · Today · R. Mehta
4 of 20 items checked20%
Procedures current and approvedPhoto
Action raised · Owner: Quality team · Due in 72 h
Records legible and retained
Action raised · Owner: Quality team · Due in 72 h
Obsolete copies removedPhoto
Action raised · Owner: Quality team · Due in 72 h
Changes logged and authorised
Action raised · Owner: Quality team · Due in 72 h
What the app does
Works offline
Inspect basements, plant rooms and rooftops. Everything syncs when you are back online.
Photo evidence
Attach photos and voice notes to every finding, right on the checklist item.
Owned corrective actions
Every failed item becomes an action with an owner, severity and due date.
AI reports
Sign off and a branded PDF, Excel or CSV report is generated and synced.
What is ISO 17025 Audit App?
ISO 17025 Audit App is a mobile tool for planning and running internal audits of a testing or calibration laboratory against ISO/IEC 17025:2017. It replaces paper checklists and spreadsheets: auditors schedule the audit, set the scope and the activities to cover, and work through a requirement-based audit tied to the standard's clauses. Impartiality and confidentiality, personnel competence, equipment and metrological traceability, method validation, measurement uncertainty, and the validity of results each have their own questions, so the audit follows the standard rather than a generic laboratory round.
Because it runs on any phone, tablet, or laptop and works offline, audits at the bench, in the calibration area, or at a remote site are never blocked, and records sync when a signal returns. Auditors capture photo, note, or record evidence against each finding, log nonconformities with a root-cause analysis, and assign corrective actions to an owner with a due date. Corrective-action verification, dashboards, and a generated audit report give the quality team the evidence trail an internal audit and management review need. It is an audit and readiness tool; it does not by itself grant or guarantee accreditation.
- Who uses it
- Quality managers, internal auditors, lab staff and process owners
- Where
- Factories, laboratories, calibration labs and service operations
- How often
- Per audit programme, with surveillance checks across the year
What the App Should Cover
A complete app covers the full internal-audit cycle: audit planning and scheduling, scope and activity selection, and a requirement-based audit mapped to the standard's clauses. It should assess impartiality and confidentiality, the structural requirements, and the resource requirements (personnel competence, facilities and environmental conditions, equipment, metrological traceability, and externally provided products and services). The process requirements follow: review of requests, selection and validation of methods, sampling, handling of test and calibration items, technical records, evaluation of measurement uncertainty, ensuring the validity of results, reporting, complaints, and nonconforming work. Management-system requirements, internal audits, and management review close the loop, with evidence capture, nonconformities, root-cause analysis, corrective actions with owners and due dates, verification, and audit report generation throughout.
How to Use ISO 17025 Audit App
An audit only helps if every auditor records each requirement the same way. Follow these steps to run an ISO 17025 audit:
- 1Plan the audit: set the scope, the testing or calibration activities to cover, the schedule, and the clauses to assess.
- 2Run the requirement-based audit on a phone, tablet, or laptop, recording a result and evidence against each clause, including traceability, method validation, and the validity of results.
- 3Raise nonconformities as you find them, record the root-cause analysis, and assign a corrective action to an owner with a due date.
- 4Work offline where signal is poor; records sync automatically when reconnected, so bench and remote-site audits are never blocked.
- 5Verify corrective actions, generate the audit report, and roll findings up for the internal audit programme and management review.
What an ISO 17025 Audit Covers
This audit checks a testing or calibration laboratory against ISO/IEC 17025: impartiality and confidentiality, personnel, facilities and equipment, metrological traceability, methods and validation, measurement uncertainty, the validity of results, reporting, and the management system. Auditors record a result and evidence on each clause, work offline where signal is poor, and raise nonconformities with corrective actions. So the audit becomes a traceable evidence pack for the internal audit programme and management review.
What gets checked
- Impartiality and confidentiality
- Personnel competence and authorisation
- Facilities and environmental conditions
- Equipment and metrological traceability
- Method selection, verification and validation
- Sampling and handling of test or calibration items
- Measurement uncertainty and validity of results
- Reporting, complaints and nonconforming work
- Management system, internal audit and management review
Common defects
- Traceability chain broken or reference standards overdue
- Method used outside its validated scope
- Measurement uncertainty not evaluated or reported
- Nonconformities without root cause or verified corrective action
Evidence to capture
- Photo, note, or record evidence against each clause
- Nonconformity records with root-cause analysis
- Corrective actions with owner, due date, and verification
- Generated audit report and audit tracking
Standards and regulations that apply: ISO/IEC 17025:2017, the laboratory's own management system documentation, your accreditation body and applicable requirements.
How ISO 17025 Audit App Runs an ISO 17025 Audit
Check Each Requirement
The ISO 17025 audit template lists the requirements to be checked.
Evidence Every Finding
Auditors attach photo proof for each ISO 17025 nonconformity.
Close and Report
Nonconformities become corrective actions and the ISO 17025 audit report generates automatically.
What ISO 17025 Teams Fix When Every Requirement Has a Recorded Result
ISO 17025 work breaks down the moment evidence leaves the form. These are the problems ISO 17025 Audit App is built to remove, and what the team gets back when it does.
Drag to compare a day before and after InspectWrk.
A failed item is noted during a routine audit. Nobody owns it, no date is set, and the next audit finds the same problem on the same ISO 17025. The ISO 17025 issue is logged, not closed.
Where it breaks
- Failed ISO 17025 items noted but never assigned to anyone
- No due date on an ISO 17025 fix, so nothing is ever overdue
- The ISO 17025 fix is marked done with no proof it happened
What changes
- Every failed ISO 17025 item becomes an owned corrective action
- Closure needs an ISO 17025 verification photo before sign-off
- Overdue actions escalate automatically
There is no live view of ISO 17025 status across sites. The first sign that something failed on the ISO 17025 is a client call or an incident, by which point the problem is already public.
Where it breaks
- No live view of ISO 17025 status across sites
- ISO 17025 problems surface as complaints, not as data
- ISO 17025 risk is invisible until it becomes an incident
What changes
- Live multi-site dashboard of ISO 17025 completion and open issues
- ISO 17025 risk scoring flags sites trending to failure
- Configurable dashboards filter ISO 17025 results by site and date
Each auditor writes up ISO 17025 findings in a different format. When someone asks for the evidence behind a nonconformity and proof it was closed, the trail is spread across notes, photos, and email.
Where it breaks
- ISO 17025 findings written up in a different format by each auditor
- Requirements skipped with no record that they were assessed
- Nonconformity evidence and closure kept in separate places
What changes
- Every ISO 17025 requirement listed in the audit template
- A recorded result and photo evidence for each requirement
- Each nonconformity tracked to verified closure
See the AI behind ISO 17025 Audit App.
Everything your field team records during ISO 17025 audit, from photos and voice notes to sign-off, InspectWrk turns into a finished report automatically.
02 / 05Voice to textVOICE AI
Speak. AI Writes It Down.
Inspectors speak their observations in any language. AI transcribes and fills the form in real time.
Completely hands-free in the field.
03 / 05Auto reportsREPORT AI
AI Writes the Report. PDF and Excel, Instantly.
The moment an inspection is submitted, AI summarises the findings and builds a branded PDF report and an Excel sheet for you.
No manual reporting. No copy-paste.
04 / 05IntegrationsINTEGRATIONS
Connect Your Existing Tools.
InspectWrk integrates with the tools your team already uses, including Zoho, Microsoft 365, and SAP.
No double entry.
05 / 05Live dashboardLIVE DATA
Live Dashboard. Every Site. Always On.
Your operations team sees completion rates, open issues, and compliance scores across all sites in real time.
No chasing updates.
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Questions aboutthis app
Still unsure? See it on your own checklist in a 30-minute demo.
Book a Free DemoIt is a mobile tool for planning and running internal audits of a testing or calibration laboratory against ISO/IEC 17025:2017. It replaces paper checklists with a requirement-based audit, captures evidence against each clause, and tracks nonconformities and corrective actions to closure. InspectWrk works offline and generates the audit report, so the internal audit programme stays on schedule for the laboratory's testing and calibration activities.
Yes. The audit maps to the ISO 17025 clauses, including impartiality and confidentiality, personnel competence, equipment and metrological traceability, method selection and validation, measurement uncertainty, ensuring the validity of results, and reporting. Auditors record a result and evidence on each requirement, raise nonconformities with a root-cause analysis, and assign corrective actions with owners and due dates.
Yes. Audits run on any phone, tablet, or laptop offline, and records sync automatically when a signal returns, so audits at the bench, in the calibration area, or at a remote site are never blocked. Findings and corrective actions are tracked on a dashboard, so the internal audit programme can be scheduled and followed in one place.
No. It is an internal-audit and readiness tool. It helps you assess conformity to the standard, capture evidence, and close nonconformities, but accreditation is granted by an accreditation body after their own assessment. Confirm specific requirements against ISO/IEC 17025 and your accreditation body's rules rather than treating any item as universally mandatory.
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