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Checklist and audit software for quality management teams

Checklist and audit software for quality management teams

With Lumiform you can ensure that your teams run consistent quality checks and manage non conformities so you stay audit ready and compliant.

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Trusted by quality teams to standardize audits, CAPAs, and reporting

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Scattered quality data hides real non conformities

Deviations are scattered across tools

Audit findings get lost in emails, Excel files, and folders, so you lose track of which issues were raised, which actions were agreed, and whether tasks closed on time.

Audit readiness is built on manual chasing

Evidence for ISO 9001 or customer audits sits in physical folders, drives and ad hoc reports, so when auditors ask for proof you have trouble locating relevant data.

CAPAs drift without traceable ownership

Corrective and preventive actions start as notes or messages with no shared log of owners, deadlines, or proof of completion, so the same deviations return in audits.

How Lumiform supports your quality management

With Lumiform you can build checklists, capture findings on mobile and generate audit-ready reports to make sure that all actions, issues and non conformities are tracked so you can kickstart real improvements.

1. Build audit ready quality and process checklists

Quality managers create and update checklists without developer help. Start from your existing forms or templates, then add sections, weights, and knock out criteria so quality issues fail an audit immediately while inspectors keep a simple workflow.
  • No code checklist builder
  • Supports ISO 9001 structures
  • Weights and knock out items
1. Build audit ready quality and process checklists

2. Capture findings on site (and even offline)

QM teams complete checks on phones or tablets directly on the shop floor, at goods receipt, or in the warehouse and can add photos, batch numbers, or notes on the spot. Offline mode keeps audits running with zero signal and syncs results automatically when a connection returns.
  • Works fully offline
  • Photos and batch data on site
  • One app for all audits
2. Capture findings on site (and even offline)

3. Turn issues into actionable follow-ups

Deviations or failed questions automatically create corrective and preventive actions. Each action gets an owner, deadline, and required proof of completion with reminders to keep actions moving.
  • Auto created CAPAs
  • Owners and deadlines
  • Evidence required at closure
3. Turn issues into actionable follow-ups

4. Report across sites and stay ISO audit ready

Dashboards show issues, action status, and audit scores across products, lines, and locations. You can filter by site, supplier, or process to see trends and weak points. Bulk export lets you pull complete, audit proof documentation to PDF or Excel when auditors or customers request evidence.
  • Cross site quality dashboards
  • Deviations and CAPA trends
  • Bulk export to PDF or Excel
4. Report across sites and stay ISO audit ready
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What changes when your quality management runs in one tool

Teams using Lumiform for quality checks report less admin work and fewer issues.

31%

faster completion of quality audits and checks

36%

fewer open issues per audit cycle

41%

improvement in CAPA on time completion

Lumiform covers your quality checks, ISO 9001 audits, CAPAs, and supplier reviews

From shop floor checks and ISO 9001 audits to CAPAs and supplier reviews, Lumiform keeps your quality workflows in one place.

Quality control operations

Teams replace paper QC forms with guided digital checklists for in process and final inspections. Results, photos, and signatures are saved in one place so you can trace which batches, lines, or shifts produced specific defects.
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ISO 9001 audits

Quality managers run internal ISO 9001 audits against defined clauses and processes. Non conformities and observations turn into tracked actions, and audit trails show what was checked, by whom, and which findings are still open.
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Non conformance tracking

Non conformities from inspections, complaints, or production issues are logged with photos, batch data, and impact. Each case gets an owner, deadline, and CAPA so you can see which problems keep recurring and how long they take to resolve.
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Corrective and preventive action

CAPAs are created from failed checks during quality inspections, are assigned to the right person, and tracked through to closure. Attach root cause analysis, photos, and documents so you have a full trail for management review and audits.
View details

Six Sigma audit

Project teams document DMAIC projects, from problem definition and measurement plans to implemented improvements and control checks. Data from inspections feeds directly into analysis so you can track defect rates and process capability in one environment
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Kaizen processes

Frontline teams record small improvement ideas in real time, attach photos or examples, and track approval and implementation. You avoid losing suggestions on paper or in chats and build a documented history of Kaizen activities.
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Standards your quality management is measured against

Whether you operate under EU directives, U.S. federal law, or international regulations, your quality management system is subject to these important standards.

ISO 9001

Core international standard for quality management systems. Requires defined processes, documented responsibilities, risk based thinking, internal audits, corrective action, and records that show how non conformities and improvements were handled over time.

ISO 9004

Guideline standard that extends ISO 9001 toward long term success. Focuses on performance, efficiency, and stakeholder satisfaction, supported by documented objectives, self assessments, and continual improvement activities across the quality system.

ISO/IEC 17025

Standard for testing and calibration laboratories. Requires documented methods, competence, traceability of measurements, equipment control, and detailed records so results are technically valid and accepted by regulators and customers.

EU Regulation 2017/745

European medical device regulation that replaces the old MDD. Requires manufacturers to maintain a quality management system, technical documentation, clinical evaluation, vigilance processes, and records that demonstrate product safety, performance, and post market surveillance.

FDA 21 CFR Part 820

US FDA Quality System Regulation for medical devices. Requires documented procedures for design controls, production, CAPA, complaint handling, and device history records that show each unit was built, tested, and released under controlled conditions.

IATF 16949

Automotive sector standard based on ISO 9001. Adds requirements for defect prevention, product safety, traceability, and customer specific standards, supported by process FMEAs, control plans, and documented evidence from production and supplier management.
Pricing that fits your quality management needs
Implement Lumiform for quality checks and roll it out without setup fees or long contracts so you improve quality processes.
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Real results from quality management teams like yours

See how companies replace spreadsheets and speed up quality audits with Lumiform.

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Quality

Rigterink optimizes logistics processes and accelerates reactions with Lumiform

Find out how Rigterink, a leading logistics company, has digitized paper-based processes and increased efficiency in quality management with the help of Lumiform. Here, the company shares its experiences and shows how Lumiform simplifies and optimizes everyday life at Rigterink.
Read case study Rigterink optimizes logistics processes and accelerates reactions with Lumiform
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Quality

PSL embraces digital quality assurance and saves costs

PSL GmbH revolutionizes its quality assurance with Lumiform through paperless processes, saves on complaint costs, and uses real-time data to continuously enhance the efficiency and responsiveness of its business.
Read case study PSL embraces digital quality assurance and saves costs
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Quality

Dorfinger KG opts for digital tools in daily operations

Discover how Dorfinger KG uses Lumiform to boost employee engagement and improve documentation quality.
Read case study Dorfinger KG opts for digital tools in daily operations
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Dennis Brepohl, Managing director, Rigterink

The ability to analyze data and create reports has revolutionized our quality management.

95% of companies that implement Lumiform increase their frontline teams' productivity, health, and safety

Easiest to do business with mid marketHighest adoptionEasiest AdminFast ImplementationEnterprise Highe PerformerBest ROIHigh performer Europe 2024High performer emea 2024High Performer small businessHigh performer spring 2024

Ready to use templates for your quality management

Quality control check sheet

Captures defects, process deviations, and recurring quality issues. Provides structured data for corrective action and trend analysis.

Use this template

Non conformance report (ISO 9001)

Log non conformities with photos, batch or order details, severity, and impact so your team can start root cause analysis and corrective actions with a clear record.

Use this template

Document change request form (ISO 9001)

Capture requests to change procedures, work instructions, or forms, including reason, risk, and approvals, so document control stays traceable.

Use this template

VDA 6.3 process audit checklist

Run VDA 6.3 process audits in line with automotive requirements, scoring questions and logging deviations so you can follow up findings with CAPAs.

Use this template
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View all templates

Common questions

Can we build our own audits and checklists, or does Lumiform build them for us?

You can build your own audits and checklists directly in Lumiform. The form builder lets you create sections, questions, response types, scoring, and logic without code, or import an existing structure as a starting point. Lumiform does not have to build forms for you, although the team can support during onboarding if you need help mapping existing documents into a digital format.

Are Lumiform’s checklists and audit reports accepted by auditors and compliant with standards like ISO 9001?

Lumiform helps you align with ISO 9001 and similar frameworks by giving you structured checklists, audit trails, and exportable reports. Auditor acceptance always depends on your specific certification body, but the platform is designed to document evidence, responsibilities, and CAPAs in a way that supports external audits rather than replacing their judgement.

What happens after a non-conformity or deviation is identified, does it automatically trigger a corrective action?

When a non conformity or deviation is identified, you can configure Lumiform to create a corrective or preventive action from that finding. The action links back to the original check, carries context such as photos and comments, and appears in an action list so quality teams track it through to closure instead of relying on email threads or spreadsheets.

Can I set a deadline for each individual corrective action, or only for the audit as a whole?

Corrective actions in Lumiform can have their own deadlines, not just one date for the entire audit. Each CAPA record includes an owner, due date, and status so you know which findings are on track or overdue. You can still track overall audit timing separately, but follow up work for individual findings is managed at action level rather than hidden in a general reminder.

Does Lumiform work offline when there is no WiFi or signal on-site?

Yes, the mobile app works offline, including during audits on shop floors, in warehouses, or at supplier sites without WiFi. Inspectors can complete full checklists and capture photos without a connection. Once the device reconnects, data syncs to the server so records, scores, and CAPAs are updated centrally without retyping results.

Can headquarters control and standardize checklist templates across multiple sites, while locations only customize within set limits?

Headquarters can define and publish master templates so every site uses the same audit structure. Local teams can be allowed to hide non relevant sections or add limited fields, depending on your governance rules, but they do not need to build their own forms from scratch. This keeps reports comparable while allowing some flexibility for local specifics.

Can I weight questions differently or mark certain findings as knock-out criteria that fail the whole audit?

Lumiform supports weighted scoring and knock out style questions in many setups. You can assign higher weights to critical items so they influence the total score more strongly, and you can model items that effectively fail an audit if they are not met. Exact configuration options depend on how your forms are set up, so complex schemes may need input from the Lumiform team.

Does Lumiform integrate with ERP or SAP so inspection and corrective action data flows automatically without manual re-entry?

Lumiform offers integrations and an API to move inspection and CAPA data into other systems, and SAP connectivity is often handled this way. The exact setup depends on your environment and plan, so you should confirm integration scope with Lumiform before relying on full automation, but the goal is to avoid manual re entry wherever possible.

Can I bulk-export multiple completed reports at once (e.g. to Excel or PDF), including photos?

You can export reports and underlying data from Lumiform in bulk. Many teams pull multiple audits into PDF or spreadsheet formats, often including images, for archiving, analysis, or sharing with external partners. The exact export formats and volume limits depend on your plan, so edge cases like very large image sets may require testing with your account manager.

Can suppliers or external auditors fill out forms without needing a full Lumiform account?

Suppliers or external auditors can usually complete forms shared with them without needing the same type of account as internal users. The exact process depends on your access model and plan, so you may use guest links, restricted users, or dedicated supplier accounts, but the intent is to involve external parties without giving them full internal permissions.

Other resources that might interest you

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